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Trophy Skin MicrodermMD

by Trophy Skin, Inc.

Trophy Skin MicrodermMD is a Class I device made by Trophy Skin, Inc., listed in FDA GUDID since 14 Sep 2016 (UDI-DI 00851561006006), 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 Number00851561006006 UDI-DI Date14 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  • Withdrawn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
Dermabrasion brush, rotary
Model / reference
MicrodermMD
Primary DI / UDI-DI
00851561006006
FDA product code
GFD
GMDN term
Dermabrasion brush, rotary
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dermabrasion brush, rotary

Similar devices

Other devices filed under FDA product code GFD (Dermatome).

Other devices from Trophy Skin, Inc.

See all devices from Trophy Skin, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)