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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 32 of 33

Device	Model / Reference	Registries	Class	Status
Flux-C Cervical Interbody	UU082-72-1412-10	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-11-0035	FDA UDI	Class II	Active
Momentum MIS	UU093-03-01	FDA UDI	Class II	Active
Momentum MIS	UU091-55-0060	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-56-1211-10	FDA UDI	Class II	Active
uNion MAX	UU201-01-0013	FDA UDI	Class II	Active
Momentum	UU051-00-7540	FDA UDI	Class II	Active
uNion Cervical Plate System	UM191-01-06	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-72-1211-07	FDA UDI	Class II	Active
uNion Cervical Plate System	UM170-00-11	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-3516	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1916-08	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-3530	FDA UDI	Class II	Active
Momentum	UU051-11-6550	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-61-0055	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-20-4525	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-01-03	FDA UDI	Class II	Active
Momentum	UU051-55-0035	FDA UDI	Class II	Active
Momentum	UU051-11-8560	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-56-1412-06	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-70-5512	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-3516	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-20-4530	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-31-4012	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-41-5535	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-3510	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-01-4028	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-21-4545	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-04-04	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-00-01	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-4012	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-3536	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-01-4036	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-11-4012	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-60-0110	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-40-4535	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-00-4030	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0201	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0108	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-15-0031	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-40-5545	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-40-5525	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-50-0000	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-20-4550	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-40-0031	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-21-4525	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-4036	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-60-0010	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-40-5550	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-4026	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.