Contract manufacturerSTAR PORT INC (Denver, CO)ColoradoGeneral and plastic surgeryClass I
STAR PORT INC
Contract manufacturer ยท Denver, CO
FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified
- FDA registration
- 3036035308 (openFDA record; or search FDA's registration database)
- FEI number
- 3036035308
- Registered for
- FDA registration year 2026
- Establishment types
- Manufacturer; Contract manufacturer
- Owner or operator
- Star Port Inc (FDA owner/operator no. 10092674)
- Registered address
- 835 JASMINE ST, Denver, CO 80220
- Contract listings
- 4 device listings, 4 product codes, first listed Feb 5, 2025
- 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 |
|---|---|---|---|---|---|
| MDA | Elastomer, Silicone, For Scar Management | Class I | General and plastic surgery | Contract manufacturing | Feb 5, 2025 |
| NAD | Dressing, Wound, Occlusive | Class I | General and plastic surgery | Contract manufacturing | Feb 5, 2025 |
| NAE | Dressing, Wound, Hydrogel Without Drug And/Or Biologic | Class I | General and plastic surgery | Contract manufacturing | Feb 5, 2026 |
| PFP | Silicone Hydrogel For Scar Management | Class I | General and plastic surgery | Contract manufacturing | Dec 25, 2025 |