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VersiQuad 0234112500

by Stryker Corp.

VersiQuad 0234112500 (234-112-500) is a tendon stripper (FDA Class I; FDA product code HRT, Stripper, Surgical) made by Stryker Corp., listed in FDA GUDID since 16 Jul 2026 (UDI-DI 07613327651164), 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 Number07613327651164 UDI-DI Date16 Jul 2026ListedStatusListed 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  • Withdrawn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
VersiQuad
Generic name
Tendon stripper
Model / Ref / Catalog
0234112500, 234-112-500
Primary DI / UDI-DI
07613327651164
FDA product code
HRT
GMDN term
Tendon stripper
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HRT (STRIPPER, SURGICAL).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

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