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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 19 of 33

Device	Model / Reference	Registries	Class	Status
uNion Cervical Plate System	UM155-45-10	FDA UDI	Class II	Active
Momentum	UU051-00-8550	FDA UDI	Class II	Active
uNion Cervical Plate System	UM190-40-05	FDA UDI	Class II	Active
uNion Cervical Plate System	UM170-00-12	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-4016	FDA UDI	Class II	Active
Momentum	UU051-01-1045	FDA UDI	Class II	Active
Momentum MIS	UU091-60-5180	FDA UDI	Class II	Active
uNion Cervical Plate System	UM191-02-04	FDA UDI	Class II	Active
Momentum	UU052-11-0055	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0105	FDA UDI	Class II	Active
uNion Cervical Plate System	UM101-01-26	FDA UDI	Class II	Active
uNion MAX	UU202-06-0010	FDA UDI	Class II	Active
uNion Cervical Plate System	UM151-40-12	FDA UDI	Class II	Active
Momentum	UU052-12-0065	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-01-4032	FDA UDI	Class II	Active
Momentum MIS	UU091-55-5110	FDA UDI	Class II	Active
Momentum	UU051-11-7555	FDA UDI	Class II	Active
Momentum	UU051-00-7550	FDA UDI	Class II	Active
Momentum MIS	UU994-90-01	FDA UDI	Class I	Active
Momentum MIS	UU091-11-8545	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-04-00	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-06-1916-06	FDA UDI	Class II	Active
uNion MAX	UU201-03-0051	FDA UDI	Class II	Active
Momentum	UU051-01-8550	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-20-01	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-21-4550	FDA UDI	Class II	Active
Momentum	UU051-11-5540	FDA UDI	Class II	Active
Momentum	UU051-01-8545	FDA UDI	Class II	Active
Momentum	UU062-81-0065	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1211-09	FDA UDI	Class II	Active
uNion MAX	UU201-41-4016	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1614-07	FDA UDI	Class II	Active
Momentum MIS	UU091-60-0080	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0106	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-41-5555	FDA UDI	Class II	Active
Momentum	UU051-01-5540	FDA UDI	Class II	Active
Momentum MIS	UU091-11-8535	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-70-1412-11	FDA UDI	Class II	Active
Momentum	UU052-30-0104	FDA UDI	Class II	Active
Momentum MIS	UU091-55-5130	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-11-0140	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1614-06	FDA UDI	Class II	Active
Momentum MIS	UU091-60-0050	FDA UDI	Class II	Active
Momentum MIS	UU091-55-5350-L	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-56-1211-08	FDA UDI	Class II	Active
Momentum MIS	UU091-11-5555	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-11-4026	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-72-1211-11	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1916-09	FDA UDI	Class II	Active
Momentum MIS	UU092-60-0100	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.