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Forceps 24-388-16-07

by KLS-Martin L.P.

Forceps 24-388-16-07 is a Class I device made by KLS-Martin L.P., listed in FDA GUDID since 26 Sep 2018 (UDI-DI 00888118032232), 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 Number00888118032232 UDI-DI Date26 Sep 2018ListedStatusListed 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  • Withdrawn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
Forceps
Generic name
Dressing/utility forceps, scissors-like, reusable
Model / reference
24-388-16-07
Primary DI / UDI-DI
00888118032232
FDA product code
DWS
GMDN term
Dressing/utility forceps, scissors-like, reusable
Device class
Class I
Regulation number
870.4500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dressing/utility forceps, scissors-like, reusable

Similar devices in this category

Other devices filed under Dressing/utility forceps, scissors-like, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)