FDA device listing
4mm Probe 90,Calibrated Probe,Curved Hip Probe,Curved Probe,GFS Small Probe,Hip Angled Probe,Hip Curved Probe,Hip…
FDA device listing 1955273336 · TAG Medical products corporation LTD
Key facts
| Proprietary names | 4mm Probe 90,Calibrated Probe,Curved Hip Probe,Curved Probe,GFS Small Probe,Hip Angled Probe,Hip Curved Probe,Hip Probe,Hip Probe 90,Hip Probe, 90,Latarjet, Small Probe,ParallelPortal Probe,Probe 30,Probe 30°,Probe 3mm.,Probe 4mm.,Probe 90,Probe 90°,Probe Straight,Shoulder Probe Biomet |
|---|---|
| Owner/operator | TAG Medical products corporation LTD |
| Owner/operator number | 9004870 |
| Product codes | HXB |
| Device names | HXB - Probe |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | T.A.G. MEDICAL PRODUCTS CORPORATION LTD |
| Establishment registrations | 8043971 |
| FEI numbers | 1000272060 |
| 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