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Scar Esthetique 60000

by Scar Heal

Scar Esthetique 60000 is a Class I device made by Scar Heal, listed in FDA GUDID since 16 Apr 2025 (UDI-DI 00642790600000), 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 Number00642790600000 UDI-DI Date16 Apr 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  • Withdrawn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
Scar Esthetique
Generic name
Scar-management dressing, single-use
Model / Ref / Catalog
60000
Primary DI / UDI-DI
00642790600000
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
Size
Total Volume — 60 Milliliter

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 Scar Heal

See all devices from Scar Heal →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)