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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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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005532635
- DUNS Number
- —
Catalogue (1623)
Page 11 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-50-1412-08 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-05 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-28 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1412-08 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1916-12 | FDA UDI | Class II | Active |
| Momentum | UU051-02-7560 | FDA UDI | Class II | Active |
| Momentum | UU052-85-0030 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1211-09 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0050 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-06 | FDA UDI | Class II | Active |
| Momentum | UU052-20-0101 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-55-0300 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM140-40-18 | FDA UDI | Class II | Active |
| Momentum | UU051-11-7545 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4512 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1412-06 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3528 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0043 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1211-12 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4030 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-08 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0120 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5130-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1614-06 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4010 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1614-09 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4024 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1211-11 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-16 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM145-45-20 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-00 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1614-09 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1412-09 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1412-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-05 | FDA UDI | Class II | Active |
| Momentum | UU051-10-5540 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM143-45-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM140-40-12 | FDA UDI | Class II | Active |
| Momentum | UU051-02-6530 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4514 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4518 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1412-10 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4524 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0100 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-20-0100 | FDA UDI | Class II | Active |
| Momentum | UU051-56-1500 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1412-07 | FDA UDI | Class II | Active |
| uNion MAX | UU201-01-0011 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM144-40-14 | 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. |