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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
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005532635
- DUNS Number
- —
Catalogue (1623)
Page 17 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU052-62-0090 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-01-4026 | FDA UDI | Class II | Active |
| Momentum | UU051-20-8100 | FDA UDI | Class II | Active |
| Momentum | UU051-01-4550 | FDA UDI | Class II | Active |
| Momentum | UU051-01-4525 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4022 | FDA UDI | Class II | Active |
| Momentum | UU051-21-1090 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0040 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-04-01 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1412-12 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-9080 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1412-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-18 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-4530 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1211-06 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-5540 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3530 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4032 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3538 | FDA UDI | Class II | Active |
| Momentum | UU051-80-0007 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0085 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1614-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1211-06 | FDA UDI | Class II | Active |
| Momentum | UU051-21-9110 | FDA UDI | Class II | Active |
| Momentum | UU051-02-7535 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-03-1605 | FDA UDI | Class II | Active |
| Momentum | UU051-70-0001 | FDA UDI | Class II | Active |
| Momentum | UU051-72-8889 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-04-64 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-12 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-55-0301 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0075 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1916-11 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4524 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-3526 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0040 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0080 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-5540 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-02-01 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1614-11 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1211-06 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-10-4535 | FDA UDI | Class II | Active |
| uNion MAX | UU202-18-30 | FDA UDI | Class II | Active |
| Momentum | UU052-85-0040 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM151-40-14 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0050-L | FDA UDI | Class II | Active |
| Momentum | UU051-72-4060 | FDA UDI | Class II | Active |
| Momentum | UU052-10-0010 | FDA UDI | Class II | Active |
| uNion MAX | UU201-04-0068 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-5535 | 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. |