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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 26 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU051-02-8550 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-01-4038 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1916-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM151-40-20 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1614-10 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5290-L | FDA UDI | Class II | Active |
| Momentum | UU051-02-1055 | FDA UDI | Class II | Active |
| Momentum | UU051-02-5545 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0045 | FDA UDI | Class II | Active |
| Momentum | UU051-21-1100 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM180-00-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM155-45-16 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-3532 | FDA UDI | Class II | Active |
| Momentum | UU052-60-0101 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-10 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-03-1300 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-10 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-31-0070 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1916-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1211-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-02-02 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-20-0300 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1614-05 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3514 | FDA UDI | Class II | Active |
| Momentum | UU051-72-1112 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5210-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1614-11 | FDA UDI | Class II | Active |
| Momentum | UU051-10-8555 | FDA UDI | Class II | Active |
| Momentum | UU051-02-8545 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0040 | FDA UDI | Class II | Active |
| Momentum | UU051-25-0060 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-06 | FDA UDI | Class II | Active |
| Momentum | UU062-81-0045 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-31-4032 | FDA UDI | Class II | Active |
| Momentum | UU051-71-8889 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3526 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-21-5525 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4024 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0070 | FDA UDI | Class II | Active |
| Momentum | UU051-00-4540 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3528 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-04-84 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0065 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1211-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-40 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1211-11 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-18 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4024 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1412-09 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4020 | 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. |