# SUPREME SCREW PRODUCTS

FEI: 3015336263
Status: Active
Establishment types: Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner/operator: Supreme Screw Products (#10081122)

Address: 10 Skyline Dr, Plainview, NY, US



## Products

Total registered: 2
Top product codes: GCJ, NAY
Regulation §: 876.1500

Proprietary names: da Vinci Xi 12mm & Stapler Bladeless Obturator, Long, da Vinci Xi 12mm & Stapler Bladeless, Obturator, Standard

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015336263%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015336263