QUALITY CONTROL · B2B MANUFACTURING
Quality Starts With Clear Requirements.
Red light therapy devices checked against the specifications agreed for your order.
Made in our own Dongguan factory, with internal quality checks for every batch and agreed customer or third-party inspection support.
AGREED REQUIREMENTS
Agree the Reference Before Checking
Confirm the product version and acceptance criteria that apply to your order.
01
Product Configuration
Confirm the model, materials, dimensions, light configuration and controls.
02
Sample & Specifications
Use the agreed specifications and, where needed, an approved sample as the production reference.
03
Acceptance Criteria
Agree inspection items, applicable tolerances and additional buyer requirements.
Consistency means meeting the agreed requirements and tolerances.
03 / FACTORY CHECKS
Checks for Your Selected Model
Review the checks and conditions that apply to your selected product.
Light Operation & Burn-In
For your model, confirm the burn-in duration, operating mode and available records.
The image shows products in operation; confirm the duration, conditions and available records for your model.
Light Component Checks
Review which light, power and control functions are checked for your configuration.
The photo shows illuminated mask components at a workbench. Checks are confirmed by model.
Bending Checks for Flexible Products
For a flexible product, confirm the bending method, cycle count and acceptance limits.
Shown: a flexible light component held in bending equipment. Applicability depends on the product.
Review Electrical & Temperature Conditions
Equipment photographs show the available scene. Confirm the method, operating conditions and records needed for your selected model.
ELECTRICAL SETUP
Power & Operating Conditions
Confirm the supply, input conditions and light or control functions to be checked for your configuration.
TEMPERATURE REVIEW
Measurement Points & Duration
Agree the operating mode, measurement locations, duration and acceptance criteria before requesting results.
BEFORE SHIPMENT
Check the Product and the Complete Order
Every batch undergoes internal quality checks before shipment.
01
Appearance & Workmanship
Visible finish, assembly and fit.
02
Model & Function
Order configuration and applicable light, power and control checks.
03
Dimensions & Materials
Requirements and tolerances agreed for the product.
04
Accessories & Instructions
Included components and approved instructions.
05
Packaging & Quantity
Labels, carton details and quantities for your order.
Inspection items, methods and sampling coverage are confirmed for each order.
MODEL-SPECIFIC DOCUMENTS
Review the Document and Its Scope
Review the document scope, listed models and destination market for your product.
Redacted document previews. Company names are partially redacted in these previews. Full documents and certificate-holder details are available on request. Applicability depends on the product model and scope.
ISO 13485:2016
Scope shown: sales of Class II medical devices within the scope of qualification (export only). Certificate No. 62825MDQM11943. Printed validity: 13 Nov 2025–12 Nov 2028.
CE / LVD Document
Selected red light lamp models, as listed in this conformity document. Review the listed models and referenced test report.
RoHS Document
Selected foot-wrap models, as listed in this document. Review the referenced sample and report scope.
FCC Supplier’s Declaration
Selected red light blanket models, as listed in this supplier declaration. Review the test standards and model coverage.
UKCA / EMC Document
Selected cap models, as listed in this EMC-related document. Review the stated standards and model coverage.
FDA REGISTRATION INFORMATION
On request
Review the applicable establishment record
FDA Registration Information
Ask for the applicable establishment registration and device-listing information for review. Registration is not product approval or clearance.
Product specifications and test information to request
Product Datasheets
The specifications for the device and version you plan to order.
Test Information
Results with the relevant method, distance and operating mode.
Applicable Documents
Listed models, document scope, version and target-market relevance.
For LED counts, distinguish physical beads from chips. Document availability is confirmed by model.
BUYER INSPECTION
Arrange Additional Inspection in Advance
Customer-appointed or third-party inspection is coordinated against agreed requirements and production readiness.
01
Scope & Criteria
Share the models, sampling requirements and acceptance criteria.
02
Timing & Access
Agree the inspection stage, schedule and practical access arrangements.
03
Fees & Follow-Up
Confirm costs, confidentiality and reinspection responsibilities before booking.
QUALITY FOLLOW-UP
Review the Issue and Agree the Next Step
The response depends on the issue, timing and agreed responsibilities.
01
Identify
Share the model, issue and affected quantity.
02
Review
Check the facts, impact and responsibility.
03
Agree
Confirm a practical corrective approach.
04
Recheck
Verify affected products where required.
05
Follow Up
Confirm the outcome and any further action.
Before shipment, review corrective work and applicable rechecks before deciding whether affected products can ship. After delivery, provide order details, quantities and photos or video; parts, repair or replacement are agreed after review.
08 / YOUR QUALITY REQUIREMENTS
Start With Your Product and Market.
Share the model, destination market and what you need to verify. If you have not selected a model, describe the product you need.
What to Share With Our Team
Product & Market
Model or product type, configuration and destination country.
Checks & Documents
Your inspection checklist, required reports or questions to review.
