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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 16 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Solidity Vertebral Body Replacement | UU041-03-1600 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-39 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM152-45-18 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4020 | FDA UDI | Class II | Active |
| Momentum | UU051-02-6555 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0100 | FDA UDI | Class II | Active |
| Momentum | UU051-20-8110 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4012 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-14 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-30-0075 | FDA UDI | Class II | Active |
| Momentum | UU052-11-0065 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-55-0400 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-6545 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1412-09 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0045 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1211-05 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-40-0400 | FDA UDI | Class II | Active |
| Momentum | UU051-01-4545 | FDA UDI | Class II | Active |
| Momentum | UU051-02-4525 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0090 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-20-02 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM145-45-10 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-5120 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4014 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU043-03-01 | FDA UDI | Class II | Active |
| Momentum | UU052-40-0300 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1916-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-51 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-08 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1916-05 | FDA UDI | Class II | Active |
| Momentum | UU051-20-1090 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM153-45-16 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3512 | FDA UDI | Class II | Active |
| Momentum | UU051-10-7540 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM150-40-18 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-25-3933 | FDA UDI | Class I | Active |
| Momentum | UU052-30-0101 | FDA UDI | Class II | Active |
| Momentum MIS | UU994-98-01 | FDA UDI | Class I | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-01-4040 | FDA UDI | Class II | Active |
| Momentum | UU051-02-7555 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-04-76 | FDA UDI | Class II | Active |
| Momentum | UU051-10-6535 | FDA UDI | Class II | Active |
| Momentum MIS | UU093-02-01 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1211-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1412-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM144-40-20 | FDA UDI | Class II | Active |
| Momentum | UU051-21-1070 | FDA UDI | Class II | Active |
| Momentum | UU051-01-5545 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-5550 | 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. |