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Mastisol 1

by Ferndale Laboratories, Inc. 4 variants

Mastisol 1 (0523-16) is a Class I device made by Ferndale Laboratories, Inc., listed in FDA GUDID since 19 Sep 2022 (UDI-DI 00304960523167), 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 Number00304960523167 UDI-DI Date19 Sep 2022ListedStatusListed 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  • Withdrawn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
Mastisol
Generic name
Skin surface device adhesive, sterile
Model / Ref / Catalog
1, 0523-16
Primary DI / UDI-DI
00304960523167
FDA product code
KGX
GMDN term
Skin surface device adhesive, sterile
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin surface device adhesive, sterile

Similar devices

Also classified as Skin surface device adhesive, sterile.

Other devices from Ferndale Laboratories, Inc.

See all devices from Ferndale Laboratories, Inc. →

Properties

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