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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 25 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU051-70-0002 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3540 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0110-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-05 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM144-40-12 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4028 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-03-03 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-90-0200 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-5530 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4032 | FDA UDI | Class II | Active |
| Momentum | UU062-81-0085 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-5550 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1614-11 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1412-09 | FDA UDI | Class II | Active |
| Momentum | UU052-14-0085 | FDA UDI | Class II | Active |
| Momentum | UU051-71-0001 | FDA UDI | Class II | Active |
| Momentum | UU052-30-0400 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0060 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-5170 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1614-06 | FDA UDI | Class II | Active |
| Momentum | UU051-10-5535 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-02-02 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0075 | FDA UDI | Class II | Active |
| uNion MAX | UU202-12-02 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-14-0104 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-10-4530 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0020 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-5530 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1614-08 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1412-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1412-08 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0050 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-60 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM153-45-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-48 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1614-10 | FDA UDI | Class II | Active |
| Momentum | UU052-30-0500 | FDA UDI | Class II | Active |
| Momentum | UU051-71-1116 | FDA UDI | Class II | Active |
| Momentum | UU051-02-5540 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-31-4018 | FDA UDI | Class II | Active |
| Momentum | UU052-10-0101 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0039 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-60-1412-05 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-9090 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-02 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-62-0240 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-71-0002 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5280-L | 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. |