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United States·US-MF-000025261
Last updated September 17, 2026
Information
- Country
- United States
- Address
- 10801 , Nesbitt Avenue South, Minnesota, United States
- Website
- www.stryker.com
- —
- —
- [email protected]
- Phone
- +1-6124715641
- PRRC Contact
- Jeanine Redden
- EUDAMED SRN
- US-MF-000025261
- FDA FEI Number
- 3000718467
- DUNS Number
- 968990812
Catalogue (8054)
Page 33 of 162| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tornier Flex Shoulder System | DWF339 | FDA UDI | Class II | Active |
| Made-To-Order | 9028483 | FDA UDI | Class I | Active |
| Blueprint™ Patient Specific Instrumentation | MWJ002 | FDA UDI | Class II | Unknown |
| Flex Shoulder System | DWF501 | FDA UDI | Class II | Active |
| ForeFoot STP | FHS-010-20F-18 | FDA UDI | Class II | Unknown |
| Ankle Suture Button | SYN-001-01 | FDA UDI | Class II | Unknown |
| Salto Talaris | LJU411 | FDA UDI | Class II | Unknown |
| Salto Talaris | LJV314 | FDA UDI | Class II | Unknown |
| 611 - Ankle Fusion Nail | VJU050 | FDA UDI | Class II | Unknown |
| Tornier Flex | MWG142 | FDA UDI | Class I | Active |
| Made-To-Order | 9028404 | FDA UDI | Class I | Active |
| ForeFoot STP | FHS-010-25-30S | FDA UDI | Class II | Unknown |
| Mini MaxLock Extreme™ | MXM-021-24-36 | FDA UDI | Class II | Active |
| MaxLock Extreme™ | COW-003-02 | FDA UDI | Class II | Unknown |
| Tornier Flex Shoulder System | DWF708B | FDA UDI | Class II | Active |
| Flex Shoulder System | DWF241 | FDA UDI | Class II | Active |
| Aequalis™ Flex Revive™ | ARS980921 | FDA UDI | Class II | Active |
| MaxLock Extreme™ | VAR-031-27-18 | FDA UDI | Class II | Unknown |
| Compression Staple System | STP-056-2024R | FDA UDI | Class I | Active |
| MaxTorque™ | SP-MSD-55-375F | FDA UDI | Class II | Unknown |
| Mini MaxLock Extreme™ | MXM-021-24-34 | FDA UDI | Class II | Active |
| Flex Shoulder System | DWF391A | FDA UDI | Class II | Active |
| Affiniti | 9000253 | FDA UDI | Class I | Unknown |
| NexFix | NCS-DG45 | FDA UDI | Class I | Active |
| Tornier Latitude | MKY004 | FDA UDI | Class I | Active |
| MaxTorque™ | MSD-010-55-055S | FDA UDI | Class II | Active |
| Made-To-Order | 9027884 | FDA UDI | Class I | Active |
| Tornier Perform Humeral System | MWV5360 | FDA UDI | Class I | Active |
| Tornier Perform® Anatomic Glenoid | DWE512 | FDA UDI | Class II | Active |
| Tornier Perform Humeral System | ARS1023809 | FDA UDI | Class I | Active |
| Tornier Perform | IFX817 | FDA UDI | Class I | Active |
| Aequalis Reversed | DWB948 | FDA UDI | Class II | Active |
| WAVE Calcaneal Fracture Plate™ | WPTLS26 | FDA UDI | Class II | Unknown |
| Ortholoc™ Sps | SPS118 | FDA UDI | Class II | Active |
| Aequalis Reversed Ii | DWH913 | FDA UDI | Class II | Active |
| TORNIER PERFORM™ Patient-Matched | DWJ607 | FDA UDI | Class II | Active |
| Made-To-Order | 9028328 | FDA UDI | Class I | Active |
| Made-To-Order | 9027356 | FDA UDI | Class I | Active |
| Stabilis™ | AFPCPT | FDA UDI | Class II | Unknown |
| Made-To-Order | 9028371 | FDA UDI | Class I | Active |
| CoverLoc™ Volar Plate | 0011205 | FDA UDI | Class II | Unknown |
| Mini MaxLock Extreme™ | MXM-002-MTP-PB | FDA UDI | Class II | Active |
| Made-To-Order | 9027364 | FDA UDI | Class I | Active |
| Aequalis Reversed II | MWB180 | FDA UDI | Class I | Active |
| MaxLock | MCS-175-NAP | FDA UDI | Class I | Active |
| ForeFoot STP | FHS-010-20-24L | FDA UDI | Class II | Unknown |
| Test-Salto Talaris | PPO221 | FDA UDI | Class II | Unknown |
| Tornier Perform | MWE090 | FDA UDI | Class I | Active |
| 611 - Ankle Fusion Nail | VJU095 | FDA UDI | Class II | Unknown |
| Tornier Latitude | 9030220 | FDA UDI | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Tornier SAS FR