FDA device listing
Retinal Tip 20G Microscissors Curved,Retinal Tip 20G Microscissors Straight,Retinal Tip 23G Microscissors Curved,Retinal…
FDA device listing 1561422965 · AKTIVE SRL
Key facts
| Proprietary names | Retinal Tip 20G Microscissors Curved,Retinal Tip 20G Microscissors Straight,Retinal Tip 23G Microscissors Curved,Retinal Tip 23G Microscissors Straight,Retinal Tip 25G Microscissors Curved,Retinal Tip 25G Microscissors Straight,Retinal Tip vertical 20G,Retinal Tip vertical 23G,Retinal Tip vertical 25G,TWEEZER ASYmmETRICAL 20G,TWEEZER Asymmetrical 27G,TWEEZER CUT CURVED 20G,TWEEZER CUT CURVED… |
|---|---|
| Owner/operator | AKTIVE SRL |
| Owner/operator number | 10087294 |
| Product codes | HNF |
| Device names | HNF - Scissors, Ophthalmic |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4350 |
| Review panels | Ophthalmic |
| Registered establishments | AKTIVE SRL |
| Establishment registrations | 3012481881 |
| FEI numbers | 3012481881 |
| Establishment operations | Manufacturer |
| 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