LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)
K-Number: K254007 · 2026-02-12
Device Summary
Frequently Asked Questions
What is the LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)?
LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281) is a medical device that received FDA 510(k) clearance on 2026-02-12. The listed applicant is SZ KKS Silicone&Electronic Co., Ltd.. The 510(k) number is K254007.
When did LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281) receive FDA 510(k) clearance?
LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281) received FDA 510(k) clearance on 2026-02-12, under 510(k) number K254007.
Who is the listed applicant for LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)?
The FDA 510(k) record lists SZ KKS Silicone&Electronic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281)?
The FDA product code for LED Light Therapy Silicone Face Mask (kks-225, kks-280, kks-281) is OHS.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OHS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.