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4723512

by Stryker Leibinger

4723512 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 37613327647243), 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 Number37613327647243 UDI-DI Date17 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  • Withdrawn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

Generic name
Orthopaedic bone screw (non-sliding)
Model / Ref / Catalog
4723512
Primary DI / UDI-DI
37613327647243
FDA product code
HWC
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class II
Regulation number
888.3040
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional
Size
Length — 12.0 Millimeter

Similar devices

Other devices filed under FDA product code HWC (Screw, fixation, bone).

Other devices from Stryker Leibinger

  • 92-55772

    Class II

  • 92-55773

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  • 92-55771

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  • 92-55770

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See all devices from Stryker Leibinger →

Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)