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ULRICH MEDICAL USA, INC.

Last updated September 17, 2026

Information

Country: US
Address: 3700 East Plano Parkway, Suite 200, Plano, TX, 75074
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005532635
DUNS Number: —

Catalogue (1623)

Page 3 of 33

Device	Model / Reference	Registries	Class	Status
Flux-C Cervical Interbody	UU082-62-1211-12	FDA UDI	Class II	Active
uNion MAX	UU201-41-4514	FDA UDI	Class II	Active
uNion MAX	UU201-41-4518	FDA UDI	Class II	Active
Momentum	UU051-02-5525	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-70-0103	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-06-1614-10	FDA UDI	Class II	Active
uNion Cervical Plate System	UM102-02-37	FDA UDI	Class II	Active
Momentum	UU051-72-8888	FDA UDI	Class II	Active
Momentum	UU053-05-01	FDA UDI	Class II	Active
Momentum	UU051-71-1114	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-66-1916-08	FDA UDI	Class II	Active
Momentum	UU051-00-1050	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-01-04	FDA UDI	Class II	Active
Solidity Vertebral Body Replacement	UU043-03-02	FDA UDI	Class II	Active
uNion Cervical Plate System	UM155-45-12	FDA UDI	Class II	Active
Solidity Vertebral Body Replacement	UU041-01-4772	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-52-1614-10	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-70-5008	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1614-12	FDA UDI	Class II	Active
uNion Cervical Plate System	UM150-40-16	FDA UDI	Class II	Active
Momentum	UU051-00-4535	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1412-12	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1211-10	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1211-08	FDA UDI	Class II	Active
Momentum	UU051-21-8090	FDA UDI	Class II	Active
Momentum	UU051-01-6550	FDA UDI	Class II	Active
uNion Cervical Plate System	UM180-00-18	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1211-11	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-72-1916-06	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-00-3540	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-21-5540	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-50-1614-08	FDA UDI	Class II	Active
Momentum	UU051-02-8535	FDA UDI	Class II	Active
Momentum MIS	UU092-30-0045	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-50-1916-06	FDA UDI	Class II	Active
uNion MAX	UU202-03-0004	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-72-1916-09	FDA UDI	Class II	Active
Momentum MIS	UU092-21-0200	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-66-1916-06	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-52-1916-11	FDA UDI	Class II	Active
Momentum MIS	UU091-55-0055	FDA UDI	Class II	Active
Momentum	UU051-74-3560	FDA UDI	Class II	Active
Momentum	UU051-70-5502	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-00-00	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-12-1211-06	FDA UDI	Class II	Active
uNion MAX	UU201-04-0076	FDA UDI	Class II	Active
uNion Cervical Plate System	UM101-01-22	FDA UDI	Class II	Active
uNion Cervical Plate System	UM102-04-60	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0107	FDA UDI	Class II	Active
Momentum MIS	UU092-20-0200	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.