FDA device listing
GEL CALLUS REMOVERS, CORN REMOVER, Heel Ankle Protector,GEL TOE SPACERS, CALLUS CUSHION, CALLUS REMOVER, CORN CUSHION…
FDA device listing 2002270878 · SUZHOU SUNMED CO., LTD
Key facts
| Proprietary names | GEL CALLUS REMOVERS, CORN REMOVER, Heel Ankle Protector,GEL TOE SPACERS, CALLUS CUSHION, CALLUS REMOVER, CORN CUSHION, BUNION CUSHION, CORN REMOVER, |
|---|---|
| Owner/operator | SUZHOU SUNMED CO., LTD |
| Owner/operator number | 10046764 |
| Product codes | FMP |
| Device names | FMP - Protector, Skin Pressure |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.6450 |
| Review panels | General Hospital |
| Registered establishments | SUZHOU SUNMED CO., LTD |
| Establishment registrations | 3005533873 |
| FEI numbers | 3005533873 |
| Establishment operations | 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