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Trophy Skin RejuvaliteMD

by Trophy Skin, Inc.

Trophy Skin RejuvaliteMD is a Class II device made by Trophy Skin, Inc., listed in FDA GUDID since 6 Sep 2016 (UDI-DI 00851561006013), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851561006013 UDI-DI Date6 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Trophy Skin
Generic name
Cosmetic red-light phototherapy system, professional
Model / reference
RejuvaliteMD
Description
RejuvaliteMD , Anti-Aging LED Treatment
Primary DI / UDI-DI
00851561006013
FDA product code
OHS
GMDN term
Cosmetic red-light phototherapy system, professional
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cosmetic red-light phototherapy system, professional

Similar devices

Other devices filed under FDA product code OHS (Light Based Over The Counter Wrinkle Reduction).

Other devices from Trophy Skin, Inc.

See all devices from Trophy Skin, Inc. →

Properties

  • Serial number
Other properties (14, all answered No)