FDA device listing
Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium
FDA device listing 1502866835 · DSI Dental Solutions Ltd
Key facts
| Owner/operator | DSI Dental Solutions Ltd |
|---|---|
| Owner/operator number | 10062297 |
| Product codes | KOT |
| Device names | KOT - Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3490 |
| Review panels | Dental |
| Registered establishments | DSI DENTAL SOLUTIONS LTD |
| Establishment registrations | 3016447764 |
| FEI numbers | 3016447764 |
| Establishment operations | Repackager/Relabeler |
| 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