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4761004

by Stryker Leibinger

4761004 is a Class I device made by Stryker Leibinger, listed in FDA GUDID since 17 Jul 2026 (UDI-DI 07613327643398), 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 Number07613327643398 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  • Withdrawn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
Manual orthopaedic bender, reusable
Model / Ref / Catalog
4761004
Primary DI / UDI-DI
07613327643398
FDA product code
LXH
GMDN term
Manual orthopaedic bender, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Length — 17.5 Centimeter

Similar devices

Other devices filed under FDA product code LXH (Orthopedic manual surgical instrument).

Other devices from Stryker Leibinger

  • 92-55772

    Class II

  • 92-55773

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  • 92-55771

    Class II

  • 92-55770

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See all devices from Stryker Leibinger →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)