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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 27 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum MIS | UU092-30-0065 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-03-04 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-20 | FDA UDI | Class II | Active |
| Momentum | UU051-02-7550 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1412-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4022 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1412-06 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-4040 | FDA UDI | Class II | Active |
| Momentum | UU052-60-0010 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM152-45-14 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-12 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-20-06 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5120 | FDA UDI | Class II | Active |
| Momentum | UU051-72-4055 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4012 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1916-10 | FDA UDI | Class II | Active |
| Momentum | UU051-01-7535 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-4032 | FDA UDI | Class II | Active |
| Momentum | UU051-20-9090 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-1110 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1412-07 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1916-06 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1211-05 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UU994-47-02 | FDA UDI | Class I | Active |
| Momentum | UU051-55-0085-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1211-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-30 | FDA UDI | Class II | Active |
| Momentum | UU051-11-5545 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-8560 | FDA UDI | Class II | Active |
| Momentum | UU053-06-01 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4028 | FDA UDI | Class II | Active |
| Momentum | UU051-01-6560 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-31-4010 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-8070 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-10-01 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-00-90 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5250-L | FDA UDI | Class II | Active |
| Momentum | UU051-02-8555 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1211-09 | FDA UDI | Class II | Active |
| Momentum | UU051-02-5535 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1211-10 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0017 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1614-12 | FDA UDI | Class II | Active |
| Momentum | UU051-11-8550 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7550 | FDA UDI | Class II | Active |
| Momentum | UU052-70-0020 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-31-0100 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5140 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1211-06 | 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. |