TheraFace LED

FDA 510(k) K212155 · Theragun, Inc.

Substantially Equivalent

510(k) numberK212155

Submission

Device name
TheraFace LED
Applicant
Theragun, Inc.
Los Angeles, CA, US
Received
July 12, 2021
Decision date
December 21, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OHS – Light Based Over The Counter Wrinkle Reduction
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

Use of light based treatment to reduce wrinkles on the body in general or specific anatomical locations depending on the information provided.

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K261496LED Light Therapy Masks (PE748, PE749, PE756)OHS · Traditional Duplex International Trading Limited08/04/2026SE
K261482LightStim for Wrinkles (1984); LightStim for Acne (2038)OHS · Traditional Led Intellectual Properties, LLC07/31/2026SE
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K261473ChromixOHS · Traditional Termosalud S.L.07/01/2026SE
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More from Guangdong Newdermo Biotech Co., Ltd.

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Questions and answers

When was TheraFace LED cleared by the FDA?

TheraFace LED (K212155) received a 510(k) decision of Substantially Equivalent on December 21, 2021, 162 days after the submission was received.

What is the product code of K212155?

The FDA product code is OHS – Light Based Over The Counter Wrinkle Reduction, a Class II (moderate risk) device regulated under 21 CFR 878.4810.