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H&H SC2106

by Tronjen Medical Technology Inc. 2 variants

H&H SC2106 is a scar-management dressing (FDA Class I; FDA product code MDA, Elastomer, Silicone, For Scar Management) made by Tronjen Medical Technology Inc., listed in FDA GUDID since 12 Dec 2025 (UDI-DI 04719884330368), 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 Number04719884330368 UDI-DI Date12 Dec 2025ListedStatusListed 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  • Withdrawn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
H&H
Generic name
Scar-management dressing, single-use
Model / reference
SC2106
Primary DI / UDI-DI
04719884330368
FDA product code
MDA
GMDN term
Scar-management dressing, single-use
Device class
Class I
Regulation number
878.4025
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code MDA (Elastomer, Silicone, For Scar Management).

Other devices from Tronjen Medical Technology Inc.

See all devices from Tronjen Medical Technology Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)