FDA device listing
FEELER; PROBE,General Instruments,Hip Probe, 90,Hip Tissue Liberator 20,PROBE
FDA device listing 2060409593 · STRYKER CORP.
Key facts
| Proprietary names | FEELER; PROBE,General Instruments,Hip Probe , 90,Hip Tissue Liberator 20,PROBE |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Product codes | HXB |
| Device names | HXB - Probe |
| Device class | Class I |
| Classification regulations (21 CFR) | 888.4540 |
| Review panels | Orthopedic |
| Registered establishments | STRYKER EMEA Supply Chain Services, STRYKER ENDOSCOPY, TORNIER Inc., TORNIER, INC., WRIGHT MEDICAL TECHNOLOGY, INC. |
| Establishment registrations | 1043534, 1649390, 2936485, 3004983210, 3008837339, 3010667733 |
| FEI numbers | 1043534, 2936485, 3000718467, 3004983210, 3008837339, 3010667733 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer, Foreign Exporter |
| 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