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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 9 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum MIS | UU091-60-5190 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4036 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-01-07 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0045-L | FDA UDI | Class II | Active |
| Momentum | UU051-70-5501 | FDA UDI | Class II | Active |
| Momentum | UU051-11-5525 | FDA UDI | Class II | Active |
| Momentum | UU053-07-01 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-62-0400 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-14-0202 | FDA UDI | Class I | Active |
| Momentum MIS | UU091-20-8110 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7545 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-72-1916-11 | FDA UDI | Class II | Active |
| Momentum | UU051-00-6560 | FDA UDI | Class II | Active |
| Momentum | UU994-84-01 | FDA UDI | Class I | Active |
| Momentum | UU051-80-0009 | FDA UDI | Class II | Active |
| Momentum | UU051-11-7550 | FDA UDI | Class II | Active |
| uNion MAX | UU201-42-4012 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM140-40-10 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-69 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM142-45-10 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4520 | FDA UDI | Class II | Active |
| Momentum | UU051-10-5545 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-02-04 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM101-02-46 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1614-07 | FDA UDI | Class II | Active |
| Momentum | UU051-02-6535 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-20-9110 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4032 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0080 | FDA UDI | Class II | Active |
| Momentum | UU051-01-5525 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-02-1610 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-3534 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM144-40-10 | FDA UDI | Class II | Active |
| Momentum | UU051-01-7550 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM170-00-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-01-24 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4522 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-62-1211-09 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5170 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5240-L | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5200 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM142-45-14 | FDA UDI | Class II | Active |
| Momentum | UU052-11-0040 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1412-08 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5180-L | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-00-4036 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-61-0025 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM153-45-12 | FDA UDI | Class II | Active |
| uNion MAX | UU201-03-0048 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM180-00-14 | 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. |