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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 31 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cortium Universal OCT Spinal Fixation System | UU000-00-01 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1211-07 | FDA UDI | Class II | Active |
| Momentum | UU051-02-4540 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1211-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-37 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0070-L | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM191-02-01 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-01-14 | FDA UDI | Class II | Active |
| Momentum | UU051-00-7555 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-3526 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM154-40-16 | FDA UDI | Class II | Active |
| Momentum | UU051-70-5503 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-02-32 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-70-1211-06 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-60-0035 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-08 | FDA UDI | Class II | Active |
| Momentum | UU051-02-4535 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4010 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-06-00 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-40-0501 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7555 | FDA UDI | Class II | Active |
| Momentum | UU051-01-8540 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1916-09 | FDA UDI | Class II | Active |
| Momentum | UU051-02-7545 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0120 | FDA UDI | Class II | Active |
| Mambo | UU994-91-01 | FDA UDI | Class I | Active |
| uNion Cervical Plate System | UM154-40-12 | FDA UDI | Class II | Active |
| Momentum | UU052-10-0020 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-12-0001 | FDA UDI | Class II | Active |
| Momentum | UU051-01-1055 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1916-08 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-20-5540 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1412-05 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM152-45-20 | FDA UDI | Class II | Active |
| Momentum | UU052-11-0085 | FDA UDI | Class II | Active |
| Momentum | UU052-50-1030 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-02-1310 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU994-97-45 | FDA UDI | Class I | Active |
| Solidity Vertebral Body Replacement | UU041-01-1927 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0100 | FDA UDI | Class II | Active |
| Momentum | UU051-00-5545 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-05-00 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM154-40-14 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4516 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1211-09 | FDA UDI | Class II | Active |
| Momentum | UU051-70-0006 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-50-0200 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0090 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1412-06 | 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. |