FDA device listing
PREFIT10 KEP 3.5,PREFIT10 KEP 4.1,PREFIT10 KEP 5.0,PREFIT10 KEX 5.0,PREFIT10 KEX 6.5,PREFIT14 KEP 3.5,PREFIT14 KEP…
FDA device listing 1035201308 · Schweizer Feinwerktechnik GmbH
Key facts
| Proprietary names | PREFIT10 KEP 3.5,PREFIT10 KEP 4.1,PREFIT10 KEP 5.0,PREFIT10 KEX 5.0,PREFIT10 KEX 6.5,PREFIT14 KEP 3.5,PREFIT14 KEP 4.1,PREFIT14 KEP 5.0,PREFIT14 KEX 5.0,PREFIT14 KEX 6.5,SCREW KEP 3.5/4.1/5.0 |
|---|---|
| Owner/operator | Schweizer Feinwerktechnik GmbH |
| Owner/operator number | 10093456 |
| Product codes | NHA |
| Device names | NHA - Abutment, Implant, Dental, Endosseous |
| Device class | Class II |
| Classification regulations (21 CFR) | 872.3630 |
| Review panels | Dental |
| Registered establishments | SCHWEIZER FEINWERKTECHNIK GMBH |
| Establishment registrations | 3039397999 |
| FEI numbers | 3039397999 |
| Establishment operations | Contract 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