FDA device listing
Bone collector,Bone collector extractor,Bone collector stopper,Connector pin,Depth pin,Drill extension,Drill…
FDA device listing 1269226293 · ACH Medical Co., Ltd.
Key facts
| Proprietary names | Bone collector,Bone collector extractor,Bone collector stopper,Connector pin,Depth pin,Drill extension,Drill stopper,Handpiece connector,Hex driver,Machine screw driver,Mount hold,Octa driver,Parallel pin,Protect cap,Ratchet adaptor,Ratchet wrench,Solid driver,Torque wrench |
|---|---|
| Owner/operator | ACH Medical Co., Ltd. |
| Owner/operator number | 10043821 |
| 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 | ACH Medical Co., Ltd. |
| Establishment registrations | 3009848796 |
| FEI numbers | 3009848796 |
| 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