Is this your brand? Sign in to claim ownership.

ULRICH MEDICAL USA, INC.

Last updated September 17, 2026

Information

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

Catalogue (1623)

Page 22 of 33

Device	Model / Reference	Registries	Class	Status
Flux-C Cervical Interbody	UU082-56-1412-10	FDA UDI	Class II	Active
Momentum	UU051-21-8100	FDA UDI	Class II	Active
uNion Cervical Plate System	UM143-45-16	FDA UDI	Class II	Active
uNion MAX	UU201-21-4522	FDA UDI	Class II	Active
Momentum	UU000-00-00	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-12-1916-08	FDA UDI	Class II	Active
uNion MAX	UU201-21-4024	FDA UDI	Class II	Active
Momentum MIS	UU091-20-1100	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-4030	FDA UDI	Class II	Active
uNion MAX	UU202-03-01	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-52-1916-12	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-50-1916-08	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-04-03	FDA UDI	Class II	Active
Momentum MIS	UU091-60-5200	FDA UDI	Class II	Active
Momentum	UU051-55-0065-L	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-3532	FDA UDI	Class II	Active
uNion Cervical Plate System	UM101-02-24	FDA UDI	Class II	Active
Momentum	UU062-84-0106	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-72-1614-09	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-12-1412-11	FDA UDI	Class II	Active
Momentum MIS	UU091-10-4550	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-52-1211-07	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-10-00	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1614-11	FDA UDI	Class II	Active
uNion MAX	UU201-01-0009	FDA UDI	Class II	Active
uNion MAX	UU000-00-01	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-66-1412-12	FDA UDI	Class II	Active
Momentum	UU051-55-0060-L	FDA UDI	Class II	Active
Momentum	UU052-85-0020	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU082-62-1614-06	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-4012	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1614-05	FDA UDI	Class II	Active
uNion Cervical Plate System	UM143-45-18	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU073-03-04	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-10-4022	FDA UDI	Class II	Active
Momentum	UU051-70-0004	FDA UDI	Class II	Active
Momentum	UU052-50-0030	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-40-0150	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-21-4530	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-61-0120	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-00-3536	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-00-1412-06	FDA UDI	Class II	Active
Flux-C Cervical Interbody	UU081-06-1211-07	FDA UDI	Class II	Active
Momentum	UU051-55-1500	FDA UDI	Class II	Active
Momentum	UU051-00-6530	FDA UDI	Class II	Active
Momentum	UU052-61-0070	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-31-4028	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-4026	FDA UDI	Class II	Active
Momentum	UU051-72-3555	FDA UDI	Class II	Active
Momentum	UU051-11-6555	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.