Contract manufacturerSUPREME SCREW PRODUCTS (Plainview, NY)New YorkGastroenterology and urologyGeneral and plastic surgeryClass II
SUPREME SCREW PRODUCTS
Contract manufacturer ยท Plainview, NY
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3015336263 (openFDA record; or search FDA's registration database)
- FEI number
- 3015336263
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer for export only; Contract manufacturer
- Owner or operator
- Supreme Screw Products (FDA owner/operator no. 10081122)
- Registered address
- 10 Skyline Dr, Plainview, NY 11803
- Contract listings
- 6 device listings, 3 product codes, first listed Mar 18, 2021
- Certification
- Not verified. We have no certification data for this facility yet.
Devices listed as contract work
Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.
| Product code | Device (FDA name) | Class | Category | Role | First listed |
|---|---|---|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | Class II | Gastroenterology and urology | Contract manufacturing | Mar 18, 2021 |
| GDW | Staple, Implantable | Class II | General and plastic surgery | Contract manufacturing | Mar 18, 2021 |
| NAY | System, Surgical, Computer Controlled Instrument | Class II | Gastroenterology and urology | Contract manufacturing | Mar 18, 2021 |