FDA device listing
Appliance, fixation, nail/blade/plate combination, multiple component,TEMPFIX EXTERNAL FIXATION SYSTEM/TEMPFIX EXTERNAL…
FDA device listing 1830844990 · Tecomet
Key facts
| Proprietary names | Appliance, fixation, nail/blade/plate combination, multiple component,TEMPFIX EXTERNAL FIXATION SYSTEM/TEMPFIX EXTERNAL FIXATION SYSTEM, MR SAFE |
|---|---|
| Owner/operator | Tecomet |
| Owner/operator number | 1828464 |
| Product codes | KTT, LXT |
| Device names | KTT - Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, LXT - Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite |
| Device class | Class II |
| Classification regulations (21 CFR) | 888.3030 |
| Review panels | Orthopedic |
| Registered establishments | SYMMETRY MEDICAL MANUFACTURING INC, SYMMETRY MEDICAL MANUFACTURING INC. |
| Establishment registrations | 1828464, 3005061536 |
| FEI numbers | 1828464, 3005061536 |
| 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