Hamilton Devices · CCELL® Hardware · 2026

Compliance & Quality

Hardware authenticity, supplier qualification, analytical heavy-metals safety, and market readiness for authentic CCELL® vaporization hardware.

View the 35-page packet Request exact-SKU evidence
Partnership
10+ years with CCELL®
Fulfillment
North Carolina, U.S.
Evidence
Exact SKU · Exact record
CCELL Ceramic EVOMAX cartridge
CCELL®Ceramic EVOMAXAll-ceramic oil path

Market leadership · Engineering certainty

The uncontested benchmark in vape hardware

In an industry defined by rapid transformation, performance under pressure is what protects brand equity. Hamilton Devices connects CCELL® materials science and manufacturing discipline with direct commercial access, U.S. fulfillment, and formulation-first technical support.

01

Materials science

Platform engineering from raw ceramic sintering forward.

02

Analytical proof

Evidence matched to the exact product and decision.

03

Operational excellence

Direct access, U.S. fulfillment, and technical support.

Authentic CCELL® · Hamilton Devices partnership

Commercial strength built around the hardware

Founded in California and operating from North Carolina as a privately held commercial entity, Hamilton Devices is focused on B2B wholesale distribution and technical execution.

10+ years

CCELL® strategic partnership

A decade-long direct relationship supporting factory volume pricing and North American allocation.

Direct

Factory affordability

Direct sourcing without intermediary brokers helps Hamilton Devices deliver efficient quantity-tiered pricing.

Precision

Industrial scale and craftsmanship

Automated manufacturing capacity is paired with the micro-tolerances required for vaporization hardware.

Authentic

Factory-direct supply

Hamilton Devices sources authentic CCELL® hardware through the authorized commercial supply chain.

U.S. hub

North Carolina fulfillment

Centralized inventory supports climate-controlled staging and same-day dispatch for eligible in-stock SKUs.

Sealed

Manufacturer-packed safeguards

Factory-sealed master cartons are stored and dispatched intact through the Hamilton Devices fulfillment layer.

Technical

Formulation-first guidance

Sales engineering connects extract profile, aperture geometry, core architecture, filling, and capping controls.

Exact SKU

Evidence transparency

Certificate, declaration, laboratory, and transport requests are routed against exact product identifiers.

01
Wholesale & pricing

Commercial Sales

Volume pricing, factory allocation, rapid quotes, sample ordering, and U.S. inventory availability.

wholesale@hamiltondevices.com
02
Product & technical data

Technical Support

Hardware matching, current data sheets, exact-SKU certificate access, evidence routing, and escalation support.

support@hamiltondevices.com

Operational alignment · Supply chain teamwork

Seamless operational chain of quality

CCELL® platform innovation, Hamilton Devices commercial logistics, and licensed extraction operators each own a defined portion of the path to a controlled finished product.

ENGINEERINGCOMMERCIAL EXECUTIONMARKET RELEASE
01 · PLATFORM

CCELL® Platform Technology

Platform Engineering

Ceramic heating technology, aperture design, airway fluid dynamics.

Factory QMS

ISO 9001:2015, ISO 13485:2016, and cGMP certified manufacturing facilities.

Documented Testing

Heavy metal screens, wetted material declarations, UN 38.3 transport reports.

Product Change Notices

Design freeze, BOM revision control, material modification alerts.

Factory Traceability

Production lot coding, raw material verification, component batching.

02 · COMMERCIAL

Hamilton Devices Partnership

Commercial Access

Tier-one volume pricing, direct factory allocation, rapid quotes.

U.S. Logistics

Centralized North Carolina inventory, same-day dispatch, freight routing.

Technical Advisory

Sample distribution, technical data sheets, sales engineering support.

Document Routing

Facilitating exact-SKU certificate access and supplier questionnaires.

Receiving Control

Inbound carton inspection, shipping lot tracking, escalation routing.

03 · FINISHED PRODUCT

Licensed Brands & Extraction Operators

Formulation Optimization

Viscosity matching, terpene blending, oxidation testing.

Filling & Capping SOPs

Temperature control, needle depth, capping speed, torque spec.

Finished Product Testing

Batch COAs, state-level contaminant testing, emissions profiles.

Packaging & Labeling

State warning statements, universal symbols, child-resistant closures.

Market Authorization

State licensing, FDA ENDS/PMTA filings (where applicable), local compliance.

Integrated outcomeAuthentic hardware · qualified formulation · controlled finished product

Corporate disclosures · Hamilton Devices self-assessment

25-point corporate & quality audit matrix

Hamilton Devices answers each control directly in first person, with clear affirmative status and the stated operational or manufacturing control behind it.

25controls
04categories
100%Yes-State responses

Supplier self-assessment · not an independent certification

Category 01

Corporate Governance & Supply Chain Security

6 controls
1.1

Is Hamilton Devices an authorized distributor of CCELL®?

YES. We are an authorized B2B commercial distributor supplying 100% authentic CCELL® products.

YES · Compliant
1.2

Are products sourced 100% direct from factory cleanrooms?

YES. All inventory is sourced directly from certified Smoore Technology manufacturing facilities.

YES · Compliant
1.3

Does Hamilton Devices operate out of its North Carolina headquarters?

YES. We operate out of our corporate headquarters and distribution hub in North Carolina.

YES · Compliant
1.4

Does Hamilton Devices command tier-one pricing via a 10+ year partnership?

YES. Our decade-long relationship with CCELL® grants us preferred commercial pricing and priority volume allocation.

YES · Compliant
1.5

Does Hamilton Devices provide dedicated technical sales engineering?

YES. In-house sales engineering teams assist customers with hardware matching and sample validation.

YES · Compliant
1.6

Are products protected by anti-counterfeit security seals?

YES. Master cartons feature serial-numbered security tape and QR authentication codes.

YES · Compliant
Category 02

Quality Management Systems (QMS) & Document Controls

6 controls
2.1

Are manufacturing facilities ISO 9001 & ISO 13485 certified?

YES. Production operates under certified ISO 9001:2015 and ISO 13485:2016 management systems.

YES · Compliant
2.2

Are cGMP guidelines followed during manufacturing?

YES. Production adheres to ISO 22716 / cGMP guidelines for cleanroom assembly and hygiene.

YES · Compliant
2.3

Is a formal Document Control procedure maintained?

YES. We maintain internal document control procedures tracking current technical data sheets (TDS).

YES · Compliant
2.4

Are compliance and quality records retained for 5+ years?

YES. All quality, shipping, lot tracking, and compliance documentation is retained for a minimum of 5 years.

YES · Compliant
2.5

Is a customer complaint handling procedure in place?

YES. Formal non-conformance SOP logs complaints, issues immediate inventory holds, and routes data to factory QA.

YES · Compliant
2.6

Is a formal CAPA system active for non-conformances?

YES. Standardized CAPA protocol requires root-cause analysis (5-Why) and resolution within 30 days.

YES · Compliant
Category 03

Materials, Calibration & Inbound Quality Control

6 controls
3.1

Are wetted materials tested for heavy metals via ICP-MS?

YES. Raw materials and oil-contact wetted components undergo ICP-MS heavy metal screening by ISO 17025 labs.

YES · Compliant
3.2

Are CCELL® ceramic cores 100% lead-free?

YES. CCELL® heating elements utilize proprietary, lead-free unglazed porous ceramic sintered above 1300°C.

YES · Compliant
3.3

Are plastic tanks food-grade and biocompatible?

YES. PCTG polymer and borosilicate glass reservoirs meet FDA 21 CFR / EU 10/2011 food-contact standards.

YES · Compliant
3.4

Is test equipment calibrated with N.I.S.T. traceability?

YES. Measuring and automated resistance testing equipment is calibrated on regular schedules with N.I.S.T. traceability.

YES · Compliant
3.5

Are production lots inspected under ANSI/ASQ Z1.4?

YES. Factory final-lot release operates to ANSI/ASQ Z1.4 (ISO 2859-1) sampling targeting AQL 0.65 for Major Defects; Hamilton receiving adds 100% security-seal and carton-integrity inspection.

YES · Compliant
3.6

Is unbroken lot traceability maintained on shipments?

YES. Outbound orders link customer POs directly to manufacturer master lot numbers printed on packaging.

YES · Compliant
Category 04

Facilities, Cleanroom Sanitation & Post-Market SOPs

7 controls
4.1

Are core components assembled in Class 100,000 cleanrooms?

YES. Core sub-assembly takes place inside Class 100,000 (ISO Class 8) cleanrooms to prevent contamination.

YES · Compliant
4.2

Are verified multi-stage sanitation SOPs active?

YES. Cleaning includes medical-grade ethanol washing, UV material sterilization, cleanroom air-showers, and ozone treatments.

YES · Compliant
4.3

Is pest control executed by certified 3rd-party vendors?

YES. Warehousing maintains non-chemical pest monitoring executed by certified commercial vendors.

YES · Compliant
4.4

Is inventory staged in climate-controlled environments?

YES. North Carolina warehousing maintains temperatures between 15°C–25°C (<60% RH) to preserve silicone seals.

YES · Compliant
4.5

Are master cartons dispatched factory-sealed and intact?

YES. Cartons arrive sealed from factory cleanrooms and are stored and shipped intact to minimize handling and contamination risk.

YES · Compliant
4.6

Are dedicated retained samples archived for 6+ months?

YES. Factory quality teams archive dedicated retained samples for a minimum of 6 months per production lot.

YES · Compliant
4.7

Are Product Change Notices (PCN) issued for engineering changes?

YES. Material or design modifications trigger a formal PCN communicated to active contract accounts.

YES · Compliant

Factory standards · Cleanroom excellence

Uncompromising manufacturing standards

Authentic CCELL® hardware distributed by Hamilton Devices is produced through documented management systems, cleanroom controls, automated screens, and lot-release sampling.

CCELL® factory controls

Manufacturer systems remain attributed to the named certificate holder, site, product family, date, and exact issued record.

Certified system

ISO 9001:2015

Certified quality management governing factory operations, supplier controls, and process consistency.

Certified system

ISO 13485:2016

Certified medical-device quality management governing cleanroom assembly lines and component purity.

Certified system

cGMP compliance

Manufacturing facilities adhere to ISO 22716 / cGMP guidelines enforced by hygiene protocols.

100% screen

Core resistance

Every ceramic heating core undergoes automated electrical resistance screening before sub-assembly against the stated 1.4Ω ± 0.1Ω nominal tolerance.

ISO Class 8

Cleanroom assembly

Cartridge sub-assembly takes place inside Class 100,000 (ISO Class 8) cleanrooms.

Lot release

AQL 0.65 target

Final lot-release sampling follows ANSI/ASQ Z1.4 / ISO 2859-1 controls targeting AQL 0.65 for major defects.

100%automated resistance screen

Every ceramic heating core is screened before sub-assembly against the stated nominal tolerance.

0.65major-defect AQL target

Lot-release sampling is stated against ANSI/ASQ Z1.4 / ISO 2859-1 production controls.

Manufacturer reference pathways: Safety · Research · Technology · Manufacture. The exact issued record controls product-specific reliance.

Logistics security · Hygiene controls

North Carolina warehouse integrity

Hamilton Devices complements manufacturer cleanroom controls with disciplined storage and dispatch of factory-sealed master cartons.

01

Medical-grade ethanol wash

Multi-stage component cleaning utilizes medical-grade ethanol for bactericidal and anti-fungal protection.

02

Air-shower and UV sterilization

Raw materials undergo air-shower processing and UV sterilization before cleanroom entry.

03

Nightly ozone treatments

Factory storage areas undergo industrial ozone sanitation treatments to reduce airborne microorganisms.

04

Climate-controlled staging

Hamilton Devices states that its North Carolina warehouse maintains 15°C–25°C and below 60% relative humidity.

Hamilton Devices warehouse control

Factory-sealed in · Factory-sealed out

Master cartons arrive factory-sealed from CCELL® cleanrooms and are stored and dispatched intact. SKU, carton condition, lot code, storage history, and outbound shipment records are matched when evidence is requested.

Evidence register · Documentation integrity

Manufacturing certificate register

Nine active record pathways connect buyers to the manufacturer-held systems and exact-product evidence summarized in the final packet.

HD-REG-001

QMS Certificate

Active · On file
Issuing body / lab
SGS / TÜV SÜD
Covered scope
CCELL® Manufacturing Facilities
Standard / regulation
ISO 9001:2015 Quality Management
HD-REG-002

Medical QMS

Active · On file
Issuing body / lab
TÜV SÜD
Covered scope
Cleanroom Assembly Lines
Standard / regulation
ISO 13485:2016 Medical Devices
HD-REG-003

Environmental QMS

Active · On file
Issuing body / lab
SGS
Covered scope
Facility Operations
Standard / regulation
ISO 14001:2015 Environmental System
HD-REG-004

Heavy Metals Test

Active · On file
Issuing body / lab
Intertek / Eurofins
Covered scope
CCELL® Cartridges (TH2 / M6T / EVO)
Standard / regulation
Heavy Metals ICP-MS Screen
HD-REG-005

Food Contact Test

Active · On file
Issuing body / lab
SGS
Covered scope
PCTG Tanks & Silicone Seals
Standard / regulation
FDA 21 CFR / EU 10/2011
HD-REG-006

RoHS Compliance

Active · On file
Issuing body / lab
SGS
Covered scope
Cartridges & Battery Assemblies
Standard / regulation
EU RoHS Directive 2011/65/EU
HD-REG-007

REACH SVHC

Active · On file
Issuing body / lab
SGS
Covered scope
Hardware Components & Plastics
Standard / regulation
EU REACH Regulation (EC) 1907/2006
HD-REG-008

Battery Transport

Active · On file
Issuing body / lab
UN 38.3 Test Lab
Covered scope
Integrated Battery Devices (Palm, Silo)
Standard / regulation
UN Manual of Tests & Criteria 38.3
HD-REG-009

Electrical Safety

Active · On file
Issuing body / lab
UL / Intertek
Covered scope
Battery Charging Circuits
Standard / regulation
UL 8139 / CE-EMC Standards

Exact-SKU evidence · Scope matching

The record must match the hardware in hand

Hamilton Devices uses a standardized context card so the scope of an analytical report is visible before a buyer relies on it.

Hamilton Devices Evidence Context CardUnderlying issued report controls
Evidence ID
HD-EV-2026-TH210-HM
Document type
Analytical Laboratory Test Report (ICP-MS Heavy Metals)
Issuing lab
Intertek Testing Services (ISO 17025 Accredited)
Named holder
Shenzhen Smoore Technology Limited
Product covered
CCELL® TH210 Cartridge (1.0mL, PCTG Tank, 2.0mm Aperture)
Test method
EPA 6020B / Acid Digestion ICP-MS
Result
PASS — Cadmium, Lead, Arsenic, Mercury Below LOR
Report date
January 15, 2026
Access class
Controlled Distribution (available through Hamilton Devices Technical Support)
Limitations
Valid only for empty, unfilled hardware under test conditions.
01

Product identity

Hamilton Devices SKU, manufacturer model, capacity, configuration, and closure.

02

Manufacturing identity

Revision or BOM, lot or date code, named holder, site, and product family.

03

Decision identity

Destination market, test method, report date, intended use, and review deadline.

Standards suite · 01 — Manufacturing quality

Manufacturing quality & certified systems

Authentic CCELL® hardware is produced under certified management systems that eclipse industry norms — from factory operations and supplier controls to cleanroom assembly and hygiene practice.

Certified QMSISO 90012015 · Quality Management

Certified Quality Management System governing factory operations, supplier controls, and process consistency across CCELL® manufacturing facilities.

HD-REG-001Active · On file
Medical Device QMSISO 134852016 · Cleanroom Assembly

Certified Medical Device Quality Management System governing cleanroom assembly lines and component purity.

HD-REG-002Active · On file
Environmental SystemISO 140012015 · Facility Operations

Certified Environmental Management System governing facility operations at partner manufacturing sites.

HD-REG-003Active · On file
Hygiene PracticecGMPISO 22716 · Cleanroom Hygiene

Manufacturing facilities adhere to ISO 22716 / cGMP guidelines enforced by strict hygiene protocols, air-shower processing, and UV sterilization.

Factory Program

Operational quality controls

100% Resistance ScreenEvery ceramic heating core is screened before sub-assembly against the 1.4Ω ± 0.1Ω nominal tolerance.
AQL 0.65 Lot ReleaseFinal production lot release operates under ANSI/ASQ Z1.4 (ISO 2859-1) sampling plans targeting AQL 0.65 for Major Defects.
Class 100,000 CleanroomCartridge sub-assembly takes place inside Class 100,000 (ISO Class 8) cleanrooms.

Summary presentation of manufacturer-held records — the exact issued certificate, declaration, report, or test summary controls product-specific reliance.

Standards suite · 02 — Material safety

Material safety & food-contact standards

Extract quality means nothing if hardware degrades it. Every wetted (oil-contact) material across CCELL® platforms is governed by international food-contact and substance-control standards.

Food-Contact MaterialsFDA 21 CFR+ EU 10/2011 · Wetted Parts

PCTG polymer and borosilicate glass reservoirs meet FDA 21 CFR and EU 10/2011 food-contact standards for oil-contact use.

HD-REG-005Active · On file
Substance ControlRoHSDirective 2011/65/EU

Cartridges and battery assemblies certified compliant with the EU RoHS Directive restricting hazardous substances.

HD-REG-006Active · On file
SVHC ScreenedREACHRegulation (EC) 1907/2006

Hardware components and plastics screened against the EU REACH SVHC candidate lists.

HD-REG-007Active · On file

Wetted materials

Mouthpiece optionsZirconia ceramic, food-grade natural wood, or BPA-free polycarbonate.
Reservoir housingMedical-grade borosilicate glass (TH2 Series) or PCTG food-grade polymer (M6T Series).
Heating core assemblyUnglazed porous ceramic, embedded NiCr heating coil, and lead-free brass airway with specified finish.
Sealing systemMedical-grade fluorosilicone and food-grade silicone gaskets. No adhesives touch the oil pathway.

Material declarations must be matched to the exact reservoir, mouthpiece, seal, core, finish, capacity, revision, and lot being purchased.

Standards suite · 03 — Heavy metals testing

Heavy metals testing & screening results

Analytical MethodICP-MSEPA 6020B · Heavy Metals

Empty CCELL® cartridges are screened by ISO 17025 accredited laboratories using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) per EPA Method 6020B. Results are measured against the California DCC action levels for inhalable products (4 CCR § 15723) — the strictest widely-adopted benchmark in U.S. cannabis.

Lead (Pb)

< 0.05 µg/g typical

CA DCC action level · 0.5 µg/g (inhalable)

Pass · Compliant

Cadmium (Cd)

< 0.01 µg/g typical

CA DCC action level · 0.2 µg/g (inhalable)

Pass · Compliant

Arsenic (As)

< 0.01 µg/g typical

CA DCC action level · 0.2 µg/g (inhalable)

Pass · Compliant

Mercury (Hg)

< 0.005 µg/g typical

CA DCC action level · 0.1 µg/g (inhalable)

Pass · Compliant

Scope distinction: DCC action levels apply to representative samples of cannabis products. Empty-hardware results and finished-product compliance are distinct scopes — the licensed brand remains responsible for finished-product testing.

Standards suite · 04 — Electrical & transport

Electrical safety & global transport

Battery-powered devices distributed by Hamilton Devices incorporate multi-layer electronic circuit protections and lithium-ion cells certified for global transit.

Transport TestedUN 38.3Lithium Battery · T.1–T.8

Integrated lithium-ion batteries pass all eight tests under the UN Manual of Tests and Criteria, Part III, subsection 38.3, documented by transport test summaries.

HD-REG-008Active · On file
Design AlignedUL 8139Vape Electrical Safety

Battery systems incorporate secondary overcharge, short-circuit, and thermal cutoff protections aligned with UL 8139 safety standards.

HD-REG-009Active · On file
EMC DirectiveCEEMC 2014/30/EU

Battery devices comply with EU Directive 2014/30/EU for electromagnetic compatibility.

HD-REG-009Active · On file
Emissions Class BFCCPart 15 · Digital Device

Charging circuitry complies with FCC Part 15 digital device radiation limits.

Device Compliance

UN 38.3 test sequence · all eight passed

T.1Altitude
T.2Thermal
T.3Vibration
T.4Shock
T.5Short Circuit
T.6Impact / Crush
T.7Overcharge
T.8Forced Discharge

UN 38.3 is transport testing documented by a test summary; it is not a general product certification. “Aligned with UL 8139” does not mean UL Listed or Classified.

Standards suite · At a glance

Standards at a glance

The core manufacturing, material, electrical, and transport standards behind authentic CCELL® hardware — in one view. Every seal is a Hamilton Devices summary mark tied to the certificate register.

Certified QMSISO 90012015 · Quality Management
HD-REG-001
Medical Device QMSISO 134852016 · Cleanroom Assembly
HD-REG-002
Environmental SystemISO 140012015 · Facility Operations
HD-REG-003
Hygiene PracticecGMPISO 22716 · Cleanroom Hygiene
Factory Program
Substance ControlRoHSDirective 2011/65/EU
HD-REG-006
SVHC ScreenedREACHRegulation (EC) 1907/2006
HD-REG-007
EMC DirectiveCEEMC 2014/30/EU
HD-REG-009
Emissions Class BFCCPart 15 · Digital Device
Device Compliance
Transport TestedUN 38.3Lithium Battery · T.1–T.8
HD-REG-008
Design AlignedUL 8139Vape Electrical Safety
HD-REG-009
Food-Contact MaterialsFDA 21 CFR+ EU 10/2011 · Wetted Parts
HD-REG-005
Analytical MethodICP-MSEPA 6020B · Heavy Metals
HD-REG-004

Material science · Wetted safety

Wetted materials & cartridge families

Hamilton Devices connects complete oil-contact material disclosure to the exact reservoir, mouthpiece, seal, core, finish, capacity, revision, and lot being purchased.

Ceramic EVOMAX cartridge
Ceramic EVOMAX
EVOMAX TH2 Glass cartridge
EVOMAX TH2 Glass
EVOMAX M6T Poly cartridge
EVOMAX M6T Poly
SE TH2 Glass cartridge
SE TH2 Glass
SE M6T Poly cartridge
SE M6T Poly
Easy TH2 Glass cartridge
Easy TH2 Glass
Easy M6T Poly cartridge
Easy M6T Poly

Mouthpiece options

Zirconia ceramic, food-grade natural wood, or BPA-free polycarbonate.

Reservoir housing

Medical-grade borosilicate glass (TH2 Series) or PCTG food-grade polymer (M6T Series).

Heating core assembly

Unglazed porous ceramic, embedded NiCr heating coil, and lead-free brass airway with specified finish.

Sealing system

Medical-grade fluorosilicone and food-grade silicone gaskets. No adhesives touch the oil pathway.

Analytical proof · ICP-MS screening

Lead-free ceramic and heavy-metals testing

Empty-cartridge screens are compared with California DCC inhalable cannabis-product action levels for decision context; the scopes remain distinct.

Lead (Pb)< 0.05 µg/gAction level · 0.5 µg/gPASS · Compliant
Cadmium (Cd)< 0.01 µg/gAction level · 0.2 µg/gPASS · Compliant
Arsenic (As)< 0.01 µg/gAction level · 0.2 µg/gPASS · Compliant
Mercury (Hg)< 0.005 µg/gAction level · 0.1 µg/gPASS · Compliant
ICP-MS empty-cartridge results compared with California DCC inhalable action levels
AnalyteDCC action levelEmpty cartridge resultStatus
Lead (Pb)0.5 µg/g< 0.05 µg/gPASS · Compliant
Cadmium (Cd)0.2 µg/g< 0.01 µg/gPASS · Compliant
Arsenic (As)0.2 µg/g< 0.01 µg/gPASS · Compliant
Mercury (Hg)0.1 µg/g< 0.005 µg/gPASS · Compliant

Formulation matching · Sales engineering

Technical qualification before scale

Approved guidance connects the extract profile to hardware geometry, current data sheets, sample testing, and a controlled fill-and-cap process.

01 · Selection workflow

From extract profile to commercial order

  1. 01Share extract profile
  2. 02Receive hardware specification
  3. 03Evaluate technical data sheets
  4. 04Order test sample kit
  5. 05Test fill and cap SOP
  6. 06Finalize order and ship
02 · Fill and cap controls

Technical operating guidelines

01

Extract filling temperature

Maintain oil between 45°C–60°C (113°F–140°F) during dispensing as the stated starting range.

02

Dispensing needle placement

Position the needle inside the reservoir without contacting the center airway shroud, maintaining 1.0mm clearance from the bottom seal.

03

Immediate capping window

Press or screw mouthpieces onto filled cartridges within 2–3 minutes of dispensing to establish the internal vacuum lock.

04

Capping torque recommendation

Screw-on mouthpieces use a stated starting range of 2.5–3.5 in-lbs (0.28–0.40 Nm).

05

Ceramic core saturation window

Allow filled cartridges to rest upright for 24 hours at 20°C–25°C before initial use.

03 · Viscosity matrix

Oil profile and hardware geometry

Starting-point viscosity and hardware selection matrix
ExtractcP @ 25°CTerpenesApertureCoreCapping
Distillate (High Purity)50,000–100,000+3%–5%2.0 mmStandard CCELL® CoreWithin 3 minutes
Live Resin / Terp Heavy15,000–40,0007%–12%1.6–1.8 mmCCELL® EVO CoreWithin 2 minutes
Live Rosin (Solventless)20,000–50,0005%–10%1.8–2.0 mmCCELL® EVO CoreImmediate capping
Liquid Diamonds60,000–120,0004%–8%2.0 mmHigh-Flow CCELL® CoreWithin 3 minutes

Regulatory boundaries · Battery transport

Market and battery readiness

Component design, transport testing, conformity pathways, and finished-product responsibilities must remain matched to the exact configuration and market.

01

State cannabis and botanical extracts

Empty hardware supplied by Hamilton Devices is intended for legal state-regulated cannabis, hemp, and botanical extract pre-fills. Licensed operators control finished-product compliance.

02

Child-resistant special packaging

Press-on and screw-on mouthpieces are designed to support 16 CFR § 1700.20 protocols when correctly locked onto matching cartridges; the exact finished package controls.

03

California Proposition 65

Material inputs do not replace an exposure-based Proposition 65 analysis. The responsible business evaluates the exact filled product, exposure, warnings, and market.

UN 38.3 · T.1–T.8

Lithium-battery transport tests

Request the current test summary for the exact cell or battery type and shipped configuration.

T.1

Altitude simulation

11.6 kPa for 6 hours

T.2

Thermal test

−40°C to +72°C cycling

T.3

Vibration

7 Hz to 200 Hz

T.4

Shock

150 Gn peak

T.5

External short circuit

Direct short circuit at 55°C

T.6

Impact / crush

Heavy-mass impact testing

T.7

Overcharge

24-hour overcharge testing

T.8

Forced discharge

Reverse-current testing

Global control

CE-EMC

EU Directive 2014/30/EU electromagnetic-compatibility pathway.

Global control

FCC Part 15 Class B

Charging-circuit digital-device radiation pathway.

Global control

UL 8139 alignment

Secondary overcharge, short-circuit, and thermal-cutoff protections aligned with the standard; alignment is not a UL listing.

Global control

RoHS and REACH

Electronic-assembly restricted-substance and SVHC documentation pathways.

Process flow · Quality gates

Manufacturing, traceability & speed

Six manufacturing and inspection stages connect verified raw materials to lot-linked Hamilton Devices receiving, staging, and fulfillment.

RAW MATERIALCOREASSEMBLYQARELEASEFULFILLMENT
01CCELL® FACTORY

RAW MATERIAL INTAKE

  • Lead-Free Brass Ingot Verification (XRF Spectrum Analysis)
  • PCTG Polymer Resin Purity Screen
  • Ceramic Core Raw Powder Particle Sizing
02CCELL® FACTORY

CORE FABRICATION & SINTERING

  • High-Temperature Ceramic Sintering (1300°C Thermal Profile)
  • Embedded NiCr Heating Coil Resistance Calibration
  • Micro-Aperture Laser Drilling (Precision ± 0.02mm)
03CCELL® FACTORY

CLEANROOM SUB-ASSEMBLY

  • ISO Class 8 Cleanroom Automated Insertion
  • Food-Grade Fluorosilicone Gasket Placement
  • Center Airway Automated Threading
04CCELL® FACTORY

IN-LINE AUTOMATED QUALITY GATES

  • 100% Core Resistance Check (1.4Ω ± 0.1Ω Target)
  • Automated Airway Obstruction Air-Flow Screen
  • Visual Vision-System Scratch & Cosmetic Inspection
05CCELL® FACTORY

FINAL AQL LOT RELEASE

  • ANSI/ASQ Z1.4 Sampling (AQL 0.65 Major / AQL 1.0 Minor)
  • Vacuum Seal Retention & Pressure Decay Test
  • Master Lot Number Inkjet Marking & Security Packaging
06HAMILTON DEVICES

HAMILTON DEVICES RECEIVING & FULFILLMENT (NORTH CAROLINA HUB)

  • Inbound Master Carton Security Seal Inspection
  • WMS Lot Number Log & Quarantine Release
  • Temperature-Controlled Pallet Staging & Order Dispatch
Release logicMaterial verification → controlled assembly → measured quality gates → lot-linked U.S. fulfillment

Lot control · Technical escalation

Traceability and resolution discipline

Every shipment dispatched by Hamilton Devices is connected through the stated traceability chain.

Field 01Customer PO Number
Field 02Hamilton Devices Invoice
Field 03Carton Master Lot Code
Field 04Factory Production Run
Field 05Raw Material Heat Lot
01

Intake & Review (0–24 Hours)

Inquiry logged via support@hamiltondevices.com. Immediate stock isolation on matching lot codes in our North Carolina hub if applicable.

02

Sample Evaluation (24–72 Hours)

Customer provides unfilled and filled samples to our sales engineering team for viscosity, capping, and resistance check.

03

Factory Resolution (Day 3–10)

Samples routed to factory engineering for root-cause analysis and resolution.

04

Resolution Delivery (Day 10–14)

Technical guidance provided and replacement inventory dispatched from verified production lots.

Sourcing velocity · U.S. fulfillment

The Hamilton Devices speed advantage

Planning benchmarks are confirmed by exact inventory, order, production allocation, freight, customs, and destination.

In-stock U.S. wholesale

North Carolina inventory

1–4 days
Hamilton Devices stock
1–4 days
Competitor benchmark
1–2 weeks

Eligible in-stock orders placed before 12:00 PM ET dispatch same-day from the North Carolina fulfillment hub.

Custom OEM program

Complete custom program

5–7 weeks
Hamilton Devices program
5–7 weeks
Competitor benchmark
13–18 weeks

Pre-production, tooling, cleanroom assembly, air freight, and release are planned within the approved program benchmark.

Vector artwork & sample approval
8d
Physical sample sign-off
5d
Tooling & component sintering
12d
Cleanroom assembly & printing
8d
Air freight / express logistics
7d
Customs clearance & release
4d

Buyer intelligence · 40 FAQ repository

Technical & commercial FAQs

Search all four approved categories: commercial and logistics, quality control and testing, formulation and filling, and battery safety and regulatory questions.

40 answers shown in all decision areas

Category A

Commercial & Logistics FAQs

01Is Hamilton Devices an authorized distributor of CCELL® products?

Yes. We are an authorized B2B commercial distributor supplying 100% authentic CCELL® hardware directly from Smoore Technology, backed by a 10+ year strategic partnership.

02Where is Hamilton Devices inventory shipped from?

Domestic wholesale orders ship directly from our centralized fulfillment hub in North Carolina.

03Are prices published online guaranteed?

Published quantity-tiered prices reflect active wholesale rates. Powered by our decade-long CCELL® relationship, we deliver industry-leading volume pricing.

04What is the minimum order quantity (MOQ) for stock items?

Stock wholesale items carry low minimum order quantities (typically 50–100 units depending on SKU).

05Can Hamilton Devices ship hardware internationally?

Yes, subject to destination country import laws regarding empty vaporization hardware.

06Are evaluation samples available for testing?

Yes. Qualified commercial processors can request sample evaluation kits through our sales engineering team.

07What payment methods are accepted for wholesale orders?

We accept ACH transfer, domestic wire transfer, major credit cards, and approved commercial credit terms for established accounts.

08How are out-of-stock items backordered?

Out-of-stock SKUs are placed on priority factory allocation with estimated delivery dates confirmed at quote issuance.

09Does Hamilton Devices offer custom packaging services?

Custom packaging and custom hardware branding are available under factory-direct custom orders.

10What is the policy on damaged shipping cartons?

Shipping damage must be reported within 48 hours of receipt with freight photos for immediate insurance claim and stock replacement.

Category B

Quality Control & Testing FAQs

11Are CCELL® cartridges heavy-metal free?

CCELL® cartridges utilize lead-free brass airways and unglazed ceramic cores that test well below state and international heavy metal action levels.

12What is the ceramic core made of?

The core consists of a high-purity, inert porous ceramic formulation sintered at temperatures exceeding 1300°C.

13Are CCELL® cartridges glued together?

No. CCELL® cartridges utilize press-fit engineered seals and medical-grade silicone gaskets. No adhesives touch the oil pathway.

14What is the AQL defect standard for factory production?

Factory production operates to ANSI/ASQ Z1.4 AQL 0.65 for Major Defects and AQL 1.0 for Minor Defects.

15Does Hamilton Devices test empty hardware for heavy metals?

Heavy metal screening is conducted by accredited ISO 17025 third-party laboratories on manufacturing production lots.

16Are plastic tanks safe for high-terpene extract formulations?

CCELL® M6T plastic cartridges utilize medical-grade PCTG polymer, specifically selected for chemical resistance against terpene degradation.

17Are CCELL® production facilities ISO certified?

Yes. Manufacturing facilities hold active ISO 9001:2015, ISO 13485:2016, and ISO 14001:2015 certifications.

18What cleanroom rating is used during cartridge assembly?

Core assembly takes place in Class 100,000 (ISO Class 8) cleanrooms.

19Is a factory QMS certificate equivalent to a product certificate?

No. A QMS certificate verifies factory quality management systems; exact product compliance relies on SKU-specific test reports.

20How does Hamilton Devices handle factory design changes?

Material design modifications trigger a formal Product Change Notice (PCN) communicated to active contract accounts.

Category C

Formulation & Filling Technical FAQs

21What oil viscosity is best suited for 2.0mm apertures?

2.0mm apertures are optimized for high-viscosity distillates (50,000–100,000+ cP).

22What aperture size should be used for solventless live rosin?

Live rosin formulations perform best in 1.8mm to 2.0mm apertures using CCELL® EVO ceramic heating cores.

23What is the recommended oil filling temperature?

Recommended oil filling temperature is typically 45°C – 60°C (113°F – 140°F) to temporarily reduce viscosity during dispensing.

24Why must cartridges be capped immediately after filling?

Immediate capping (within 2–3 minutes) creates a negative pressure vacuum inside the reservoir, preventing oil from flooding the ceramic core.

25What capping torque spec should be applied to screw-on mouthpieces?

Recommended capping torque for screw-on mouthpieces is 2.5 to 3.5 in-lbs (0.28 – 0.40 Nm).

26What causes cartridge leakage from the bottom air intakes?

Leakage is typically caused by delayed capping, over-heated oil during filling, under-viscous formulations, or damaged silicone seals.

27What causes dry hits or burnt taste?

Dry hits occur when extract viscosity is too high for the selected aperture size, or when the cartridge is fired before the ceramic core fully saturates.

28How long should cartridges settle after capping before use?

Cartridges should settle upright for a minimum of 24 hours at room temperature to allow full ceramic core saturation.

29Can CCELL® cartridges be refilled?

CCELL® cartridges are designed for single-use commercial pre-fills to ensure consumer safety and prevent seal degradation.

30What storage orientation is recommended for pre-filled cartridges?

Filled cartridges should be stored mouth-upright in temperature-controlled environments (15°C–25°C).

Category D

Battery Safety & Regulatory FAQs

31Are CCELL® batteries UN 38.3 certified for air transport?

Yes. All integrated lithium-ion batteries hold valid UN 38.3 transport test summaries.

32Do Hamilton Devices batteries feature auto-draw activation?

Select models (e.g., Palm, Silo) feature pneumatically activated auto-draw sensors; other models feature button activation.

33Are CCELL® batteries UL 8139 listed?

Battery safety systems incorporate thermal and short-circuit protections aligned with UL 8139 electrical standards.

34Are press-on mouthpieces child-resistant?

Press-on mouthpieces utilize permanent locking mechanisms designed to meet PPPA child-resistance requirements when fully seated.

35Does Hamilton Devices provide Prop 65 warning stickers?

Prop 65 compliance depends on the customer's finished filled formulation; hardware components do not independently trigger Prop 65 warnings.

36What charger voltage should be used for CCELL® batteries?

Use standard 5V USB charging blocks. High-voltage fast chargers (9V/12V) should not be used.

37What is the shelf life of an empty CCELL® cartridge?

Unfilled cartridges stored in original vacuum-sealed packaging have a recommended shelf life of 24 months from manufacture date.

38How does cold weather affect battery performance?

Sub-freezing temperatures temporarily increase internal battery resistance, reducing output capacity until warmed to operating temperature.

39How can a customer request SKU-specific technical reports?

Submit exact SKU, lot number, and target market requirements to support@hamiltondevices.com.

40How does Hamilton Devices support custom branding programs?

Contact our wholesale sales team at wholesale@hamiltondevices.com to review vector artwork guidelines, custom color matching, and 5–7 week production schedules.

Claims discipline · Public guardrails

Strong claims require strong boundaries

Disciplined substantiation strengthens the sales story by keeping every statement attached to the source that supports it.

01

No evidence drift

A manufacturer certificate, component declaration, or laboratory report applies only within its named holder, site, product, revision, lot, method, and date scope.

02

No certification inflation

Transport testing, design alignment, and component features are not presented as agency approval or finished-product certification unless the exact issued record says so.

03

No finished-product transfer

Licensed brands remain responsible for formulation, filling, packaging, labeling, warnings, finished-product testing, and destination-market authorization.

Full publication master

Review the complete 35-page compliance packet

The full PDF opens in your browser and contains the complete self-assessment, register, technical matrices, FAQs, and claims-control page.

Open the packet

Data request · Evidence archive

Request the record for the hardware in hand

Provide the exact Hamilton Devices SKU, manufacturer lot if available, destination market, requested record class, and review date.

Exact SKU · Exact Record

Hardware technical data request

This request goes directly to the Hamilton Devices compliance team at support@hamiltondevices.com. Add the contact email you want the reply sent to.

8. Requested document type(s) · required

A request does not establish that a record exists, is current, matches the product, or is approved for release. If this form does not send, email support@hamiltondevices.com.

EvaluateRequest evaluation samplesProcureContact Wholesale SalesEvidenceEmail Technical Support