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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 1 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU051-01-7545 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0040 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-5545 | FDA UDI | Class II | Active |
| Momentum | UU051-21-9070 | FDA UDI | Class II | Active |
| Momentum | UU051-21-1080 | FDA UDI | Class II | Active |
| Momentum | UU051-26-0015 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-04-1600 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1211-08 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-1080 | FDA UDI | Class II | Active |
| uNion MAX | UU202-10-10 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0030-L | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0028 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5012 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0014 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-8100 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1916-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1614-05 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-09 | FDA UDI | Class II | Active |
| Modified Instrument - HXX | UU994-68-01 | FDA UDI | Class II | Active |
| Momentum | UU051-70-5504 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1211-06 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0037 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM191-02-02 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-71-0001 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM142-45-16 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-20-0200 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1916-12 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-12-0145 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-14-0102 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4034 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM155-45-18 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4524 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1412-11 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-10-0001 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1916-08 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-4545 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5516 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-18 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-01-1317 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-50-0140 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1916-11 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-10-4540 | FDA UDI | Class II | Active |
| uNion MAX | UU202-10-12 | FDA UDI | Class II | Active |
| uNion MAX | UU202-06-0008 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-40-4525 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0035 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4022 | FDA UDI | Class II | Active |
| uNion MAX | UU201-04-0084 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-42 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0042 | 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. |