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Fluoromap 81-81022

by Stryker Leibinger

Fluoromap 81-81022 is a Class II device made by Stryker Leibinger, listed in FDA GUDID since 28 Jan 2025 (UDI-DI 07613252196259), 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 Number07613252196259 UDI-DI Date28 Jan 2025ListedStatusListed 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  • Withdrawn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
Fluoromap
Generic name
Optical surgical navigation/tracking system
Model / Ref / Catalog
81-81022
Primary DI / UDI-DI
07613252196259
FDA product code
LLZ, OLO
GMDN term
Optical surgical navigation/tracking system
Device class
Class II
Regulation number
892.2050, 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)