FDA device listing
Alcon8548 (DK) - GRIESHABER ULTRASHARP Knife (Sclerotomy, Discission or Scleral Pocket)
FDA device listing 1613960172 · STERIS Corporation
Key facts
| Proprietary names | Alcon8548 (DK) - GRIESHABER ULTRASHARP Knife (Sclerotomy, Discission or Scleral Pocket) |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 10042227 |
| Product codes | HNN |
| Device names | HNN - Knife, Ophthalmic |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4350 |
| Review panels | Ophthalmic |
| Registered establishments | STERIS Schweiz AG, Synergy Health Ede BV, Synergy Health Sterilisation UK Ltd |
| Establishment registrations | 8043792, 3002807310, 3009337401 |
| FEI numbers | 3002807310, 3002808269, 3009337401 |
| Establishment operations | Contract Sterilizer |
| 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