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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 5 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-56-1412-08 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4020 | FDA UDI | Class II | Active |
| Momentum | UU052-70-0011 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-11-0030 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0090 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0030 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-09 | FDA UDI | Class II | Active |
| uNion MAX | UU202-06-0007 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1916-07 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1916-12 | FDA UDI | Class II | Active |
| Momentum | UU053-03-01 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-21-4535 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0050-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1412-06 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-63 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0060 | FDA UDI | Class II | Active |
| Momentum | UU052-61-0090 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-0080 | FDA UDI | Class II | Active |
| Momentum | UU051-02-5555 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1916-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM141-40-14 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1614-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1916-09 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-31-0080 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1412-09 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1916-10 | FDA UDI | Class II | Active |
| uNion MAX | UU201-02-0034 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1412-12 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-5555 | FDA UDI | Class II | Active |
| Momentum | UU051-20-8080 | FDA UDI | Class II | Active |
| uNion MAX | UU201-21-4016 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1916-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM153-45-20 | FDA UDI | Class II | Active |
| uNion MAX | UU202-12-04 | FDA UDI | Class II | Active |
| Momentum | UU994-94-01 | FDA UDI | Class I | Active |
| uNion MAX | UU201-22-4024 | FDA UDI | Class II | Active |
| Momentum | UU051-00-8540 | FDA UDI | Class II | Active |
| Momentum | UU051-10-6545 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0065-L | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-41-4535 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1412-08 | FDA UDI | Class II | Active |
| Momentum | UU052-50-1010 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1211-07 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0055 | FDA UDI | Class II | Active |
| Momentum | UU051-02-1050 | FDA UDI | Class II | Active |
| Momentum | UU052-50-0110 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3520 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-43 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0065 | 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. |