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Cranialmap 6000-655-100

by Stryker Leibinger

Cranialmap 6000-655-100 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 24 Aug 2016 (UDI-DI 07613252510673), 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 Number07613252510673 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  • Withdrawn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
Cranialmap
Generic name
Optical surgical navigation/tracking system
Model / Ref / Catalog
6000-655-100
Primary DI / UDI-DI
07613252510673
FDA product code
HAW
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

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See all devices from Stryker Leibinger →

Properties

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