# rms Surgical

FEI: 3010009693
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: THE CRETEX COMPANIES, INC. (#9001389)

Address: 1220 Lund Blvd, Anoka, MN, US



## Products

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

Proprietary names: V2F, Optio-C (Anterior Cervical System), Harmony Posterior, Unicompartmental Knee System Spacer Block 5 Degrees 14 Mm Thickness, TELESCOPING LOCKING BOOM, OXF MP 10DEG FMRL DRILL GUIDE, OXF MP 10DEG FMRL DRL GD MED, POST WALL IMPACTOR LEFT 24MM, STRAIGHT OSTOTOME 12MM, OSTEOTOME IMPACTOR RIGHT 24MM

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010009693%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010009693