FDA device listing
Suprathel CW,Suprathel Hand,Suprathel Wound and Burn Dressing
FDA device listing 1968574607 · Polymedics Innovations
Key facts
| Proprietary names | Suprathel CW,Suprathel Hand,Suprathel Wound and Burn Dressing |
|---|---|
| Owner/operator | Polymedics Innovations |
| Owner/operator number | 10029744 |
| Premarket submissions | K090160 |
| Product codes | QSZ |
| Device names | QSZ - Absorbable Synthetic Wound Dressing |
| Device class | Unclassified |
| Classification regulations (21 CFR) | ORCA1.QSZ |
| Review panels | General & Plastic Surgery |
| Registered establishments | POLYMEDICS INNOVATIONS, Polymedics Innovations, Inc. |
| Establishment registrations | 3007710611, 3012366156 |
| FEI numbers | 3007710611, 3012366156 |
| Establishment operations | Complaint File Establishment, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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