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TheraClear 20TC12900AA

by Theravant Corporation

TheraClear 20TC12900AA is a Class II device made by Theravant Corporation, listed in FDA GUDID since 20 Sep 2016 (UDI-DI B30520TC1290), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB30520TC1290 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
TheraClear
Generic name
Multi-modality skin surface treatment system generator
Model / Ref / Catalog
20TC12900AA, 20TC129
Primary DI / UDI-DI
B30520TC1290
FDA product code
ONF
GMDN term
Multi-modality skin surface treatment system generator
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multi-modality skin surface treatment system generator

Other devices from Theravant Corporation

See all devices from Theravant Corporation →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)