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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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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3005532635
- DUNS Number
- —
Catalogue (1623)
Page 13 of 33| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Momentum MIS | UU091-60-5160 | FDA UDI | Class II | Active |
| Momentum | UU052-63-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-4034 | FDA UDI | Class II | Active |
| Momentum | UU051-02-6560 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1614-12 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-52-1614-07 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM102-03-54 | FDA UDI | Class II | Active |
| Momentum MIS | UU092-10-0500 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-40-0060 | FDA UDI | Class II | Active |
| uNion MAX | UU203-00-00 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU073-05-01 | FDA UDI | Class II | Active |
| Momentum | UU052-61-0100 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU072-10-0012 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5150-L | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-82-1916-06 | FDA UDI | Class II | Active |
| Momentum | UU051-00-7545 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU041-03-1610 | FDA UDI | Class II | Active |
| uNion MAX | UU203-00-02 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-06-1614-05 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-66-1614-09 | FDA UDI | Class II | Active |
| uNion MAX | UU201-41-4012 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0070 | FDA UDI | Class II | Active |
| Solidity Vertebral Body Replacement | UU042-02-03 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM180-00-20 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4040 | FDA UDI | Class II | Active |
| Momentum | UU052-13-0045 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-00-1916-12 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM145-45-12 | FDA UDI | Class II | Active |
| uNion MAX | UU201-22-4022 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-7535 | FDA UDI | Class II | Active |
| Momentum | UU051-10-8550 | FDA UDI | Class II | Active |
| Momentum | UU051-01-7555 | FDA UDI | Class II | Active |
| uNion Cervical Plate System | UM153-45-18 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0110-L | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-5010 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-70-0001 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3520 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-11-4038 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU081-12-1412-07 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-71-0011 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-6550 | FDA UDI | Class II | Active |
| Momentum MIS | UU091-11-8555 | FDA UDI | Class II | Active |
| Flux-C Cervical Interbody | UU082-56-1412-07 | FDA UDI | Class II | Active |
| Momentum | UU051-60-0055 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-01-4030 | FDA UDI | Class II | Active |
| Momentum | UU051-55-0100-L | FDA UDI | Class II | Active |
| Momentum MIS | UU091-55-5170-L | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-30-4028 | FDA UDI | Class II | Active |
| Cortium Universal OCT Spinal Fixation System | UU071-10-3534 | 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. |