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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 33 of 33

Device	Model / Reference	Registries	Class	Status
Cortium Universal OCT Spinal Fixation System	UU071-61-0060	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-01-4034	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-41-5545	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-00-4026	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-60-0050	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-30-3532	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-61-0040	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-40-0041	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-41-4525	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU071-00-3538	FDA UDI	Class II	Active
Cortium Universal OCT Spinal Fixation System	UU072-20-0101	FDA UDI	Class II	Active
Navigation Module of the Momentum System	K200845	FDA 510(k)	Class II	Active
uCerv Flux-C 3D Porous Titanium Cervical Interbody	K220696	FDA 510(k)	Class II	Active
Momentum™ Posterior Spinal Fixation System	K191932	FDA 510(k)	Class II	Active
Momentum® Posterior Spinal Fixation System with G21 V-STEADY Bone Cement; Momentum® MIS Posterior Spinal Fixation System with G21 V-STEADY Bone Cement	K231809	FDA 510(k)	Class II	Active
uCerv Flux™-C 3D Porous Titanium Cervical Interbody	K241396	FDA 510(k)	Class II	Active
Momentum® MIS Posterior Spinal Fixation System	K223274	FDA 510(k)	Class II	Active
Navigation Module of the Cortium® System	K252087	FDA 510(k)	Class II	Active
uNion Cervical Plate System	K150666	FDA 510(k)	Class II	Active
Momentum® Posterior Spinal Fixation System	K251719	FDA 510(k)	Class II	Active
uNion® MAX Cervical Plate System	K240515	FDA 510(k)	Class II	Active
Solidity Vertebral Body Replacement	K181921	FDA 510(k)	Class II	Active
Cortium™	K230614	FDA 510(k)	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.