FDA device listing
Blink,INSTRUMENT TIP GUARDS,INSTRUMENT WIPES, PVA SPONGE
FDA device listing 1158436239 · Corza Medical, Inc.
Key facts
| Proprietary names | Blink,INSTRUMENT TIP GUARDS,INSTRUMENT WIPES, PVA SPONGE |
|---|---|
| Owner/operator | Corza Medical, Inc. |
| Owner/operator number | 2242450 |
| Product codes | MDM |
| Device names | MDM - Instrument, Manual, Surgical, General Use |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Blink Medical LTD, KATENA PRODUCTS, INC. |
| Establishment registrations | 1934420, 2242450, 3013602181, 3015177648 |
| FEI numbers | 2242450, 3001180016, 3013602181, 3015177648 |
| Establishment operations | Manufacturer, Repackager/Relabeler, Specification Developer |
| 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