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ULRICH MEDICAL USA, INC.

US

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
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EUDAMED SRN
—
FDA FEI Number
3005532635
DUNS Number
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Catalogue (1623)

Page 7 of 33
DeviceModel / ReferenceRegistriesClassStatus
Momentum UU052-30-0300
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-52-1916-08
FDA UDI
Class IIActive
Momentum UU052-12-0075
FDA UDI
Class IIActive
Momentum UU051-11-5550
FDA UDI
Class IIActive
Momentum UU051-01-8555
FDA UDI
Class IIActive
Momentum UU051-01-5530
FDA UDI
Class IIActive
uNion Cervical Plate System UM101-02-26
FDA UDI
Class IIActive
Momentum UU051-74-3555
FDA UDI
Class IIActive
Momentum UU051-55-0060
FDA UDI
Class IIActive
uNion MAX UU201-21-4018
FDA UDI
Class IIActive
Momentum MIS UU091-60-5130
FDA UDI
Class IIActive
uNion MAX UU202-03-0003
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-60-0120
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-70-1211-12
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-10-0020
FDA UDI
Class IIActive
Momentum UU062-81-0075
FDA UDI
Class IIActive
Momentum MIS UU091-11-6535
FDA UDI
Class IIActive
uNion Cervical Plate System UM102-03-57
FDA UDI
Class IIActive
Momentum MIS UU091-20-1090
FDA UDI
Class IIActive
Momentum UU051-11-6540
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-12-1412-12
FDA UDI
Class IIActive
Momentum UU051-01-5555
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-70-5014
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-52-1614-08
FDA UDI
Class IIActive
uNion Cervical Plate System UM170-00-01
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU994-97-30
FDA UDI
Class IActive
Flux-C Cervical Interbody UU082-82-1916-11
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-10-0002
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-00-1412-05
FDA UDI
Class IIActive
uNion Cervical Plate System UM102-03-45
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1412-10
FDA UDI
Class IIActive
Momentum MIS UU091-60-5150
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1614-06
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-50-0050
FDA UDI
Class IIActive
Momentum UU051-02-6545
FDA UDI
Class IIActive
Momentum UU051-55-0040
FDA UDI
Class IIActive
uNion MAX UU201-42-4020
FDA UDI
Class IIActive
Momentum MIS UU092-21-0100
FDA UDI
Class IIActive
Momentum MIS UU091-55-5190
FDA UDI
Class IIActive
Momentum MIS UU091-55-0045
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU073-02-01
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-11-0155
FDA UDI
Class IIActive
Momentum UU051-00-5540
FDA UDI
Class IIActive
Momentum MIS UU091-55-5160-L
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-82-1211-07
FDA UDI
Class IIActive
Momentum UU051-80-2009
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-15-0030
FDA UDI
Class IIActive
Momentum MIS UU091-20-8090
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-31-4016
FDA UDI
Class IIActive
Momentum UU051-00-4530
FDA UDI
Class IIActive

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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.

DateRecall No.ClassStatusReason
Dec 31, 2019Z-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, 2019Z-1126-2019—terminated

Certain Torque Limiting Handles in the field are beyond their 3 year calibration life.

Mar 7, 2017Z-1878-2017—terminated

Surgical technique was revised to prevent static plate screws blocking mechanisms from disassociating.