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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 30 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU052-60-0102 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0070 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM150-40-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-11 | FDA UDI | Class II | Active |
| Momentum | UU051-11-8535 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1916-07 | FDA UDI | Class II | Active |
| Momentum | UU051-71-8888 | FDA UDI | Class II | Active |
| Momentum | UU052-30-0102 | FDA UDI | Class II | Active |
| Momentum | UU051-80-2209 | FDA UDI | Class II | Active |
| Momentum | UU051-20-9110 | FDA UDI | Class II | Active |
| Momentum | UU051-02-4550 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-50-0148 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0110 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3512 | FDA UDI | Class II | Active |
| uNion MAX | UU202-05-0100 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1614-08 | FDA UDI | Class II | Active |
| Momentum | UU063-09-01 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0120-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1916-06 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-21-5530 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1412-05 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-4540 | FDA UDI | Class II | Active |
| Momentum | UU052-60-2045 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-03-05 | FDA UDI | Class II | Active |
| Momentum | UU051-10-6560 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-01-1621 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-04-02 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5340-L | FDA UDI | Class II | Active |
| Momentum | UU051-60-0090 | FDA UDI | Class II | Active |
| Momentum | UU051-10-8560 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4520 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1412-09 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-16 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-12 | FDA UDI | Class II | Active |
| Momentum | UU051-00-4550 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1211-12 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-6530 | FDA UDI | Class II | Active |
| Momentum | UU052-20-0200 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0070 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1614-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1614-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-08 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5160 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0045-L | FDA UDI | Class II | Active |
| Momentum | UU051-60-0050 | FDA UDI | Class II | Active |
| Momentum | UU051-10-8535 | FDA UDI | Class II | Active |
| uNion MAX | UU202-05-0102 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-4540 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0031 | FDA UDI | Class II | Active |
| Momentum | UU052-30-0103 | 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. |