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Wire Watch™ WW-12K

by Biotex, Inc.

Wire Watch WW-12K is a surgical drape clip (FDA Class I; FDA product code KGZ, Accessories, Catheter) made by Biotex, Inc., listed in FDA GUDID since 31 Jul 2023 (UDI-DI M710WW12K0), 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 NumberM710WW12K0 UDI-DI Date31 Jul 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Wire Watch™
Generic name
Surgical drape clip, reusable
Model / reference
WW-12K
Primary DI / UDI-DI
M710WW12K0
FDA product code
KGZ
GMDN term
Surgical drape clip, reusable
Device class
Class I
Regulation number
878.4200
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical drape clip, reusable

Similar devices

Other devices filed under FDA product code KGZ (Accessories, Catheter).

Other devices from Biotex, Inc.

See all devices from Biotex, Inc. →

Properties

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