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Detachol 1

by Ferndale Laboratories, Inc. 6 variants

Detachol 1 (0513-04) is a Class I device made by Ferndale Laboratories, Inc., listed in FDA GUDID since 19 Sep 2022 (UDI-DI 00304960513045), 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 Number00304960513045 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  • Withdrawn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
Detachol
Generic name
Patient medical adhesive remover
Model / Ref / Catalog
1, 0513-04
Primary DI / UDI-DI
00304960513045
FDA product code
KOX
GMDN term
Patient medical adhesive remover
Device class
Class I
Regulation number
878.4730
GUDID distribution status
In Commercial Distribution

Related devices

Category: Patient medical adhesive remover

Similar devices in this category

Other devices filed under Patient medical adhesive remover.

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)