# Medartis Inc.

FEI: 3009540749
Status: Active
Establishment types: Manufacture Medical Device; Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device for Another Party (Contract Manufacturer); Complaint File Establishment per 21 CFR 820.198
Owner/operator: MEDARTIS AG (#9033581)

Address: 1195 Polk Drive, Warsaw, IN, US



## Products

Total registered: 1
Top product codes: LXH
Regulation §: 888.4540

Proprietary names: APTUS and MODUS Instruments, Lapidus Cut Guide, StealthFix Intraosseous Fixation System, Lapiprep Lapidus Preparation System, Patella Clamp Head, PSN Drop Rod Adapter, BandLoc, PediFlex, PediFrag, Avenger Radial Head System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009540749%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009540749