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ScarMD 3g

by Aim Medical Inc

ScarMD 3g is a scar-management dressing (FDA Class I; FDA product code MDA, Elastomer, Silicone, For Scar Management) made by Aim Medical Inc, listed in FDA GUDID since 21 Aug 2020 (UDI-DI 00860004589730), 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 Number00860004589730 UDI-DI Date21 Aug 2020ListedStatusListed 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  • Withdrawn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
ScarMD
Generic name
Scar-management dressing, single-use
Model / reference
3g
Primary DI / UDI-DI
00860004589730
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

Related devices

Category: Scar-management dressing, single-use

Similar devices in this category

Other devices filed under Scar-management dressing, single-use.

Other devices from Aim Medical Inc

See all devices from Aim Medical Inc →

Properties

  • Supplied sterile
  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)