FDA device listing
Scar Gel (SG-03)
FDA device listing 1838030919 · Star Port Inc
Key facts
| Proprietary names | Scar Gel (SG-03) |
|---|---|
| Owner/operator | Star Port Inc |
| Owner/operator number | 10092674 |
| Product codes | PFP |
| Device names | PFP - Silicone Hydrogel For Scar Management |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4025 |
| Review panels | General & Plastic Surgery |
| Registered establishments | STAR PORT INC |
| Establishment registrations | 3036035308 |
| FEI numbers | 3036035308 |
| Establishment operations | Contract Manufacturer, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database