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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 20 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Flux-C Cervical Interbody | UU082-50-1211-09 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM150-40-10 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-12-0155 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1412-08 | FDA UDI | Class II | Active |
| Momentum | UU051-10-5555 | FDA UDI | Class II | Active |
| uNion MAX | UU202-06-0005 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0040 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4512 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-02-04 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-24 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5120-L | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-1070 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-00-91 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0101 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1614-06 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM154-40-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1614-08 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-16 | FDA UDI | Class II | Active |
| Momentum | UU052-10-0103 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0036 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1211-07 | FDA UDI | Class II | Active |
| Momentum | UU051-02-4545 | FDA UDI | Class II | Active |
| Momentum | UU051-70-5505 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1412-10 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-50-1614-10 | FDA UDI | Class II | Active |
| Momentum | UU051-25-0015 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5330-L | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-26 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-12 | FDA UDI | Class II | Active |
| Momentum | UU062-82-0085 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1916-09 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3522 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1412-12 | FDA UDI | Class II | Active |
| Momentum | UU051-10-6550 | FDA UDI | Class II | Active |
| Momentum | UU051-60-1500-L | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM143-45-20 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0030-L | FDA UDI | Class II | Active |
| Momentum | UU051-72-1111 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-06-02 | FDA UDI | Class II | Active |
| Momentum | UU062-83-0100 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1211-08 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM151-40-10 | FDA UDI | Class II | Active |
| Momentum | UU052-50-1000 | FDA UDI | Class II | Active |
| Momentum | UU051-10-7535 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM190-00-92 | FDA UDI | Class II | Active |
| Momentum | UU051-71-1111 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-6540 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1211-06 | FDA UDI | Class II | Active |
| Momentum | UU994-76-02 | FDA UDI | Class II | Active |
| Momentum | UU051-11-7535 | 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. |