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VersiQuad 0234112609

by Stryker Corp.

VersiQuad 0234112609 (234-112-609) is a manual scalpel blade (FDA Class I; FDA product code GES, Blade, Scalpel) made by Stryker Corp., listed in FDA GUDID since 16 Jul 2026 (UDI-DI 07613327651218), 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 Number07613327651218 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  • Withdrawn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
Manual scalpel blade, single-use
Model / Ref / Catalog
0234112609, 234-112-609
Primary DI / UDI-DI
07613327651218
FDA product code
GES
GMDN term
Manual scalpel blade, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GES (BLADE, SCALPEL).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)