FDA device listing
Cutimed Sorbact Dressing Pad,Cutimed Sorbact Swab,Cutimed Sorbact WCL,Leukomed Sorbact,Sorbact
FDA device listing 1351452057 · ABIGO MEDICAL AB
Key facts
| Proprietary names | Cutimed Sorbact Dressing Pad,Cutimed Sorbact Swab,Cutimed Sorbact WCL,Leukomed Sorbact,Sorbact |
|---|---|
| Owner/operator | ABIGO MEDICAL AB |
| Owner/operator number | 9004891 |
| Premarket submissions | K063059 |
| Product codes | FRO |
| Device names | FRO - Dressing, Wound, Drug |
| Device class | Unclassified |
| Classification regulations (21 CFR) | ORCA1.FRO |
| Review panels | General & Plastic Surgery |
| Registered establishments | ABIGO MEDICAL AB |
| Establishment registrations | 8043991, 3009750086 |
| FEI numbers | 3004017406, 3009750086 |
| Establishment operations | Manufacturer, Specification Developer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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