FDA Device Establishments · JSON-LD · Markdown

rms Surgical

FEI 3010009693 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active

FEI Number3010009693
Owner / OperatorTHE CRETEX COMPANIES, INC. (#9001389)
Address1220 Lund Blvd, Anoka, MN, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LXH
Regulation § (21 CFR)888.4540
Proprietary namesV2F; 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

External sources

Source: openFDA. Public-domain (CC0).