Certification coverage decides whether you can sell in a market at all. The full position, rather than a row of logos — and the documents themselves, so you can check rather than take our word for it.
Coverage
Where these can ship
- FDA — establishment registration and device listing, United States. Registration 3012161895, owner/operator 10088192
- FCC — equipment authorisation for the Bluetooth models. FCC ID 2AZKH-KAISUM (eye), 2AZKH-H1 (head)
- CE — EMC and LVD, European Economic Area
- RoHS — restricted substances, eye and head ranges tested separately
- SGS — independent factory audit, March 2026
- ISO 9001:2015 — management system, design and production of head, eye and neck massagers
FDA registration is not FDA approval or certification. The FDA does not issue or recognise certificates of registration, and we do not claim one. Registration means the facility and its device listing are on file with the FDA, which is what a US importer needs from us — and it is verifiable in the FDA’s own database.
Standards
Built to GB 4706
All devices meet GB 4706.1-2005 and GB 4706.10-2008 — the Chinese national safety standards for household electrical appliances, and for skin and hair care appliances respectively.
Test reports and certificates are available on request for any model, and we support additional market-specific testing where your destination requires it. For the lithium cell we hold CCC and Korean KC certificates — both published — plus a CB test report to IEC 62133-2, an EU Battery Regulation heavy-metals report and a RoHS ten-substance report. Those three are reports rather than certificates and are supplied in full on request; the CB report may not be reproduced in part. We do not currently hold a UN38.3 transport report.