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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 18 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-66-1614-06 | FDA UDI | Class II | Active |
| Momentum | UU051-01-6545 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-10 | FDA UDI | Class II | Active |
| Momentum | UU051-02-1045 | FDA UDI | Class II | Active |
| Momentum | UU052-10-0100 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-6560 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4516 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-10-0011 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-3530 | FDA UDI | Class II | Active |
| Momentum | UU052-60-0007 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0070 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-4545 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM191-02-03 | FDA UDI | Class II | Active |
| Momentum | UU051-80-1008 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1412-07 | FDA UDI | Class II | Active |
| Momentum | UU062-83-0103 | FDA UDI | Class II | Active |
| Momentum | UU051-00-5535 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1614-11 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5140-L | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-20-00 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1614-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0070 | FDA UDI | Class II | Active |
| Momentum | UU052-12-0085 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM145-45-16 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0075 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM143-45-14 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-70-0200 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0035-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1916-07 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0022 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-5110 | FDA UDI | Class II | Active |
| Momentum | UU052-30-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-4530 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-20-0205 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4018 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1916-09 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-21-5550 | FDA UDI | Class II | Active |
| Momentum | UU051-20-1070 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0160 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3536 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1412-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-04-02 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-50-0040 | FDA UDI | Class II | Active |
| Momentum | UU051-20-1100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5510 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0050 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-60-0045 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM144-40-16 | FDA UDI | Class II | Active |
| Momentum | UU051-70-0003 | 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. |