FDA device listing
0.5 Slot Driver,0.9 Hex Driver,1.25 Angled Driver,1.25 Hex Driver,1.2 Angled Driver,1.2 Hex Driver,Abutment Screw…
FDA device listing 1503194372 · Cybermed Inc.
Key facts
| Proprietary names | 0.5 Slot Driver,0.9 Hex Driver,1.25 Angled Driver,1.25 Hex Driver,1.2 Angled Driver,1.2 Hex Driver,Abutment Screw Driver,Anchor Pin,Anchor Sleeve,Base Metal Carrier,Bone Carrier,Bone Flatter,Bone Packer,Bone Profiler,Bone Pusher,CORE1 Guide KIT,CORE1 Guide KIT Simple,CORE1 Implant Mount,CORE1 Implant Mount Extension,CORE1 Mount Driver,CORE1 Prosthetic KIT,CORE Implant Mount,CORE Master KIT,CORE… |
|---|---|
| Owner/operator | Cybermed Inc. |
| Owner/operator number | 9048516 |
| 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 | Cybermed Inc. |
| Establishment registrations | 3003781339 |
| FEI numbers | 3003781339 |
| 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