FDA device listing
BONE MANAGEMENT,Meisinger Screwdriver,MEISINGER Spreader,myplant two Backturn Instrument,myplant two Handle…
FDA device listing 1471738405 · HAGER & MEISINGER GMBH
Key facts
| Proprietary names | BONE MANAGEMENT,Meisinger Screwdriver,MEISINGER Spreader,myplant two Backturn Instrument,myplant two Handle Laboratory,myplant two Hand Wheel,myplant two High Torque Adapter,myplant two Implant Analog,myplant two Laboratory Analog Ball Anchor,myplant two Laboratory Analog One-Piece,myplant two Open-End Wrench,myplant two Positioning Key,myplant two Ratchet,myplant two Repositioning Post,myplant… |
|---|---|
| Owner/operator | HAGER & MEISINGER GMBH |
| Owner/operator number | 8010516 |
| Product codes | NDP |
| Device names | NDP - Accessories, Implant, Dental, Endosseous |
| Device class | Class I |
| Classification regulations (21 CFR) | 872.3980 |
| Review panels | Dental |
| Registered establishments | HAGER & MEISINGER GMBH |
| Establishment registrations | 8010516 |
| FEI numbers | 3004169071 |
| 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