FDA device listing
Aequalis Fx2,Aequalis PerFORM,ALL TORNIER FORCEPS INSTRUMENTS,General Instruments,HOLDING FORCEPS,OSTEONICS,Stryker…
FDA device listing 1124900079 · STRYKER CORP.
Key facts
| Proprietary names | Aequalis Fx2,Aequalis PerFORM,ALL TORNIER FORCEPS INSTRUMENTS,General Instruments,HOLDING FORCEPS,OSTEONICS,Stryker Orthopaedics Screw Forceps |
|---|---|
| Owner/operator | STRYKER CORP. |
| Owner/operator number | 1811755 |
| Product codes | HTD |
| Device names | HTD - Forceps |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4800 |
| Review panels | General & Plastic Surgery |
| Registered establishments | HOWMEDICA OSTEONICS CORP, STRYKER ENDOSCOPY, STRYKER GmbH, TORNIER Inc., TORNIER, INC., Tornier S.A.S., WRIGHT MEDICAL TECHNOLOGY, INC. |
| Establishment registrations | 1043534, 1649390, 2249697, 2936485, 8031020, 3000931034, 3004983210, 3010667733 |
| FEI numbers | 1043534, 2936485, 3000718467, 3000931034, 3002807830, 3003070421, 3004983210, 3010667733 |
| Establishment operations | Complaint File Establishment, Manufacturer, Specification Developer, Repackager/Relabeler |
| 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