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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 21 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum | UU051-11-7560 | FDA UDI | Class II | Active |
| Momentum | UU051-20-9100 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0090 | FDA UDI | Class II | Active |
| Momentum | UU051-55-7300 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM143-45-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-09 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3534 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1916-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM145-45-14 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3540 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-14-0101 | FDA UDI | Class II | Active |
| Momentum | UU051-11-6535 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM180-00-12 | FDA UDI | Class II | Active |
| Momentum | UU052-62-0080 | FDA UDI | Class II | Active |
| Momentum | UU051-00-5555 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-10-0200 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0100 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4014 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-46 | FDA UDI | Class II | Active |
| uNion MAX | UU201-04-0080 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-03-01 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-5545 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1412-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-71-0010 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0040-L | FDA UDI | Class II | Active |
| Momentum | UU994-89-01 | FDA UDI | Class I | Active |
| Flux-C Cervical Interbody | UU082-13-0001 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5230-L | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-34 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1614-07 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4020 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-30-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4038 | FDA UDI | Class II | Active |
| Momentum | UU051-20-8070 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0110 | FDA UDI | Class II | Active |
| Momentum | UU051-00-5525 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0032 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-06 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0040 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-40-0502 | FDA UDI | Class II | Active |
| Momentum MIS | UU093-01-01 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-10-0600 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1916-07 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1211-07 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0085 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3524 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0120-L | FDA UDI | Class II | Active |
| Momentum | UU051-20-1080 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1916-08 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-13 | 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. |