FDA cleared the AMIRO Spectra 10-in-1 LED Light Therapy Mask (L3) from Shenzhen Accompany Technology Co., Ltd. on Oct 19, 2026 under K262932, a traditional 510(k). The device falls under product code OHS, Light Based Over The Counter Wrinkle Reduction, regulated at 21 CFR 878.4810 as a Class 2 device. The review panel was General, Plastic Surgery.
FDA logged the submission as received on Aug 21, 2026. The decision came 59 days later, inside the 90 FDA-day goal for a 510(k).
This is the only decision on file for Shenzhen Accompany Technology Co., Ltd. in the last 12 months of the tracker.
Questions & Answers
What did FDA clear under K262932?
K262932 is the FDA 510(k) for AMIRO Spectra 10-in-1 LED Light Therapy Mask (L3), submitted by Shenzhen Accompany Technology Co., Ltd.. FDA's decision date was Oct 19, 2026, under product code OHS (Light Based Over The Counter Wrinkle Reduction).
Who makes the AMIRO Spectra 10-in-1 LED Light Therapy Mask (L3)?
Shenzhen Accompany Technology Co., Ltd., based in Shenzhen, is the applicant of record for K262932.
How long did the K262932 review take?
FDA received the submission on Aug 21, 2026 and issued its decision on Oct 19, 2026, 59 days later.