Intertek · MDSAP
ISO 13485:2016
Design, manufacture and distribution of LED light therapy masks.
Quality & Compliance
Certified where it counts.
The platform is backed by a documented quality system and market-specific conformity files. Scans are kept in our quality system; current copies are available on request.
Documentation
The files behind the platform.
U.S. FDA · FY2025
FDA Registration
Facility registration for Shenzhen Liyoutong Technology Co., Ltd.
ENC · CE
EMC Directive 2014/30/EU
EN IEC 55014-1:2021 and EN IEC 55014-2:2021 for the LED mask platform.
ENC · FCC
47 CFR Part 15 Subpart B
Declaration of conformity for the LED mask beauty instrument.
ENC · RoHS
EU 2011/65/EU
Restriction of hazardous substances declaration for the LED mask platform.
Certificate numbers, model ranges and issuing bodies are shown on the scans. Certificates apply to the named facility and product scope; your own market may require additional steps, which are mapped at sampling.
Behind the certificates
A quality system, not a folder of PDFs.
The documents only mean something if the process behind them is repeatable. Every build follows the same documented route, from incoming parts to final inspection.
- Sample approval before production. The finish, fit and configuration are confirmed on a physical unit before the run starts.
- Traceable documentation. Test reports and declarations are filed against the product and facility they cover.
- Market route agreed early. The certification path for your target country is mapped at sampling, not left to the end.
Need a certificate copy for your market?
Tell us the product line and destination country, and we will send the relevant documents and flag anything that still needs to be arranged.
