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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 4 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-70-1412-12 | FDA UDI | Class II | Active |
| Momentum | UU051-00-8545 | FDA UDI | Class II | Active |
| Momentum | UU051-00-6545 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-5540 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-26 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1916-06 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-11 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0057 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-8080 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-4540 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0060 | FDA UDI | Class II | Active |
| Momentum | UU051-55-1500-L | FDA UDI | Class II | Active |
| Momentum | UU052-20-0102 | FDA UDI | Class II | Active |
| Momentum | UU051-11-8555 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0055-L | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM191-01-07 | FDA UDI | Class II | Active |
| Momentum | UU063-09-02 | FDA UDI | Class II | Active |
| Momentum | UU051-30-0000 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-01-3551 | FDA UDI | Class II | Active |
| Momentum | UU052-50-1020 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-32 | FDA UDI | Class II | Active |
| uNion MAX | UU202-06-0006 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-50-0400 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1916-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-31-4030 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-30-0102 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-31-4036 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU043-01-02 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-01-04 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4018 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0019 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-50-0100 | FDA UDI | Class II | Active |
| uNion MAX | UU202-03-03 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-30-0055 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1916-10 | FDA UDI | Class II | Active |
| uNion MAX | UU202-06-0009 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-50-0150 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0085-L | FDA UDI | Class II | Active |
| Momentum | UU051-21-9100 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-02-03 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5190-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1916-10 | FDA UDI | Class II | Active |
| Momentum | UU051-10-7550 | FDA UDI | Class II | Active |
| Momentum | UU051-00-1045 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1614-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1614-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-11-0001 | FDA UDI | Class II | Active |
| Momentum | UU052-12-0055 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5508 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-28 | 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. |