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6003-710-000

by Stryker Leibinger

6003-710-000 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 11 May 2023 (UDI-DI 07613327542332), 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 Number07613327542332 UDI-DI Date11 May 2023ListedStatusListed 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  • Withdrawn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
Surgical planning/navigation-enhancement system
Model / Ref / Catalog
6003-710-000
Primary DI / UDI-DI
07613327542332
FDA product code
OLO
GMDN term
Surgical planning/navigation-enhancement system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Robotic surgical navigation system application software

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  • 92-55770

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See all devices from Stryker Leibinger →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)