FDA device listing
DISPOSABLE TANO POLISHER, 20GA,DISPOSABLE TANO POLISHER, 23GA,DISPOSABLE TANO POLISHER, 25GA
FDA device listing 1180546628 · Carl Zeiss Meditec AG (Jena)
Key facts
| Proprietary names | DISPOSABLE TANO POLISHER, 20GA,DISPOSABLE TANO POLISHER, 23GA,DISPOSABLE TANO POLISHER, 25GA |
|---|---|
| Owner/operator | Carl Zeiss Meditec AG (Jena) |
| Owner/operator number | 9053564 |
| Product codes | MXY |
| Device names | MXY - Cannula, Ophthalmic, Posterior Capsular Polishing, Polyvinyl Acetal |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4350 |
| Review panels | Ophthalmic |
| Registered establishments | FCI FRANCE CHIRURGIE INSTRUMENTATION, FCI SAS, FCI SUD |
| Establishment registrations | 9615745, 3002991496, 3004467263 |
| FEI numbers | 3000314405, 3002991496, 3004467263 |
| 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