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4741002

by Stryker Leibinger

4741002 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 07613327602258), 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 Number07613327602258 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  • Withdrawn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 fixation plate, non-bioabsorbable
Model / Ref / Catalog
4741002
Primary DI / UDI-DI
07613327602258
FDA product code
HRS
GMDN term
Orthopaedic fixation plate, non-bioabsorbable
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Conditional

Similar devices

Other devices filed under FDA product code HRS (Plate, fixation, bone).

Other devices from Stryker Leibinger

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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)