# RMS CO.

FEI: 1000116116
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: THE CRETEX COMPANIES, INC. (#9001389)

Address: 8600 EVERGREEN BLVD., MINNEAPOLIS, MN, US



## Products

Total registered: 4
Top product codes: MNI, KWP, KWQ, MNH
Regulation §: 888.3070, 888.3050, 888.3060

Proprietary names: InCompass Thoracolumber Fusion System, InCompass System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000116116%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000116116