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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 8 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| uNion MAX | UU201-03-0054 | FDA UDI | Class II | Active |
| Momentum | UU051-25-0030 | FDA UDI | Class II | Active |
| Momentum | UU051-01-8535 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-30 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-00-93 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-04-72 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1412-10 | FDA UDI | Class II | Active |
| Momentum | UU051-02-8560 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1412-05 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0030 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-31-0090 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0066 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0080-L | FDA UDI | Class II | Active |
| Screwdriver | UU094-54-02 | FDA UDI | Class I | Active |
| uNion MAX | UU201-02-0026 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0075-L | FDA UDI | Class II | Active |
| Momentum | UU062-82-0045 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7560 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-09 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-11-0040 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0090 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1211-08 | FDA UDI | Class II | Active |
| uNion MAX | UU202-10-18 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0130 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4014 | FDA UDI | Class II | Active |
| uNion MAX | UU202-03-0005 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0030 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4010 | FDA UDI | Class II | Active |
| Momentum | UU051-10-7555 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0025 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1916-07 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-05 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0085 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-5530 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-4545 | FDA UDI | Class II | Active |
| Momentum | UU051-71-0000 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-02-00 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0050 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1412-11 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-20-03 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-03-02 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0065 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1412-06 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1614-08 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0040 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3522 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-02-1600 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU043-02-01 | FDA UDI | Class II | Active |
| Momentum | UU051-01-5550 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1614-11 | FDA UDI | Class II | Active |
Related Companies
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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. |