# Materialise USA, LLC.

FEI: 3005718816
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: MATERIALISE N.V. (#9029485)

Address: 44650 Helm Court, Plymouth, MI, US



## Products

Total registered: 4
Top product codes: MBH, OIY, OOG, JWH
Regulation §: 888.3565, 888.3560

Proprietary names: Bespoke Patient Specific Instruments, Materialise TKA Guides, SurgiCase Knee Planner, Materialise Knee Guides, Materialise Knee Planner, Materialise TKA Guide System, Materialise SurgiCase Knee Planner, Materialise SurgiCase Knee Module, Materialise Knee Guide System, Materialise Knee Platform

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005718816%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005718816