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Sign in to claim this brandULRICH MEDICAL USA, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 3700 East Plano Parkway, Suite 200, Plano, TX, 75074
- Website
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- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005532635
- DUNS Number
- —
Catalogue (1623)
Page 23 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU051-00-4545 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-08 | FDA UDI | Class II | Active |
| Momentum | UU051-01-8560 | FDA UDI | Class II | Active |
| Momentum | UU051-80-2211 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4520 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-4550 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1614-07 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5300-L | FDA UDI | Class II | Active |
| Momentum | UU051-02-1060 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-03-1305 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-12 | FDA UDI | Class II | Active |
| Momentum | UU051-02-6540 | FDA UDI | Class II | Active |
| Momentum | UU051-00-8555 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1614-06 | FDA UDI | Class II | Active |
| Momentum | UU051-01-6540 | FDA UDI | Class II | Active |
| Momentum | UU051-21-8070 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1412-08 | FDA UDI | Class II | Active |
| Momentum | UU051-80-1006 | FDA UDI | Class II | Active |
| Momentum | UU062-81-0040 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM154-40-20 | FDA UDI | Class II | Active |
| Momentum | UU051-80-0011 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0055 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-08 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1412-08 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-14 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0120 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM140-40-14 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-06-03 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4016 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4014 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1916-11 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-8550 | FDA UDI | Class II | Active |
| Momentum | UU052-70-0030 | FDA UDI | Class II | Active |
| Momentum | UU051-11-6530 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1211-09 | FDA UDI | Class II | Active |
| Momentum | UU053-02-01 | FDA UDI | Class II | Active |
| Momentum | UU051-21-8080 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-40-07 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1412-07 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4518 | FDA UDI | Class II | Active |
| Momentum | UU051-00-4525 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0030 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-40 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1916-11 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4018 | FDA UDI | Class II | Active |
| Momentum | UU051-80-1208 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4518 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-06 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1412-11 | FDA UDI | Class II | Active |
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 31, 2019 | Z-1350-2020 | — | terminated | Due to a production error, the weld seam of the "Locking screw for crosslink, screw-to-screw" cannot reliably transmit the required torque of 3.5 Nm during installation. |
| Mar 8, 2019 | Z-1126-2019 | — | terminated | Certain Torque Limiting Handles in the field are beyond their 3 year calibration life. |
| Mar 7, 2017 | Z-1878-2017 | — | terminated | Surgical technique was revised to prevent static plate screws blocking mechanisms from disassociating. |