FDA device listing
Kit, Surgical Instrument, Disposable
FDA device listing 1983935821 · INNOVARXI LTD.
Key facts
| Proprietary names | Kit, Surgical Instrument, Disposable |
|---|---|
| Owner/operator | INNOVARXI LTD. |
| Owner/operator number | 10091365 |
| Product codes | KDD |
| Device names | KDD - Kit, Surgical Instrument, Disposable |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | INNOVARXI LTD. |
| Establishment registrations | 3032579548 |
| FEI numbers | 3032579548 |
| Establishment operations | Foreign Private Label Distributor |
| 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