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Orthomap 6005-661-000

by Stryker Leibinger

Orthomap 6005-661-000 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 24 Aug 2016 (UDI-DI 04546540651624), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04546540651624 UDI-DI Date24 Aug 2016ListedStatusListed 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  • Withdrawn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
Orthomap
Generic name
Optical surgical navigation/tracking system
Model / Ref / Catalog
6005-661-000
Primary DI / UDI-DI
04546540651624
FDA product code
OLO
GMDN term
Optical surgical navigation/tracking system
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution

Related devices

Category: Robotic surgical navigation system application software

Other devices from Stryker Leibinger

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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)