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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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- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005532635
- DUNS Number
- —
Catalogue (1623)
Page 12 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| uNion MAX | UU202-05-0101 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1614-09 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-03-02 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1211-09 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0046 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4016 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-10-0010 | FDA UDI | Class II | Active |
| Momentum | UU051-02-5530 | FDA UDI | Class II | Active |
| Momentum | UU052-50-1040 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1916-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-24 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4516 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-03-06 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-01-03 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM150-40-14 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-40-06 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-10 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0010 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0090 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4014 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4030 | FDA UDI | Class II | Active |
| Momentum | UU052-15-0500 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-03-1310 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5320-L | FDA UDI | Class II | Active |
| Momentum | UU051-71-2000 | FDA UDI | Class II | Active |
| uNion MAX | UU202-10-24 | FDA UDI | Class II | Active |
| Momentum | UU052-20-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3510 | FDA UDI | Class II | Active |
| Momentum | UU051-11-5530 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1614-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU994-95-41 | FDA UDI | Class I | Active |
| uNion MAX | UU201-42-4514 | FDA UDI | Class II | Active |
| Momentum | UU062-84-0103 | FDA UDI | Class II | Active |
| Momentum | UU051-01-6535 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5260-L | FDA UDI | Class II | Active |
| Momentum | UU051-01-5535 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-01-2839 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM152-45-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-20 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0110 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-4550 | FDA UDI | Class II | Active |
| Momentum | UU062-81-0055 | FDA UDI | Class II | Active |
| Momentum | UU051-71-2001 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0055 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-21-5545 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0110 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0063 | FDA UDI | Class II | Active |
| uNion MAX | UU202-10-14 | FDA UDI | Class II | Active |
| Momentum | UU052-70-0021 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0024 | 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. |