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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 15 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-72-1412-08 | FDA UDI | Class II | Active |
| Cortium | CS 3932-06M | FDA UDI | Class I | Active |
| uNion MAX | UU201-42-4018 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5514 | FDA UDI | Class II | Active |
| Momentum | UU051-10-5550 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0012 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-20-0201 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4514 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4038 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5150 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-04-80 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1614-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1614-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM180-00-25 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4018 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1211-06 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM142-45-18 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0008 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1211-05 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-5525 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1916-06 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0025 | FDA UDI | Class II | Active |
| Momentum | UU051-60-1500 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-30-0101 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1211-11 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-09 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0040 | FDA UDI | Class II | Active |
| Momentum | UU053-01-01 | FDA UDI | Class II | Active |
| Momentum | UU051-00-6550 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0170 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7540 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-11 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM151-40-18 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1916-05 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0070 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3514 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1614-11 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-34 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-02 | FDA UDI | Class II | Active |
| Momentum | UU051-01-6555 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-30-0085 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-02-02 | FDA UDI | Class II | Active |
| Momentum | UU051-74-4055 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1412-11 | FDA UDI | Class II | Active |
| Momentum | UU052-20-0103 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-71-0012 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-66 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1412-12 | 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. |