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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
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Email
—
Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3005532635
DUNS Number
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Catalogue (1623)

Page 2 of 33
DeviceModel / ReferenceRegistriesClassStatus
Momentum MIS UU092-70-0100
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-06-1614-12
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-40-5535
FDA UDI
Class IIActive
Momentum UU052-20-0201
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-56-1614-09
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-06-1211-05
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-31-4014
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-06-1412-06
FDA UDI
Class IIActive
Momentum UU052-11-0045
FDA UDI
Class IIActive
uNion Cervical Plate System UM180-00-16
FDA UDI
Class IIActive
Solidity Vertebral Body Replacement UU042-01-02
FDA UDI
Class IIActive
Momentum UU051-21-9080
FDA UDI
Class IIActive
Momentum UU051-01-7540
FDA UDI
Class IIActive
Modified Instrument - LXH UU994-86-02
FDA UDI
Class IActive
Cortium Universal OCT Spinal Fixation System UU072-50-0020
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-82-1412-09
FDA UDI
Class IIActive
uNion MAX UU201-42-4522
FDA UDI
Class IIActive
Momentum UU051-74-4060
FDA UDI
Class IIActive
uNion MAX UU202-00-0000
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-82-1211-11
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-70-5506
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-21-4540
FDA UDI
Class IIActive
uNion MAX UU201-01-0021
FDA UDI
Class IIActive
uNion MAX UU202-18-15
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-66-1211-07
FDA UDI
Class IIActive
Solidity Vertebral Body Replacement UU041-02-1305
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-21-4555
FDA UDI
Class IIActive
Momentum UU051-01-1060
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU073-01-10
FDA UDI
Class IIActive
Momentum UU051-60-0045
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-66-1614-11
FDA UDI
Class IIActive
Momentum UU051-00-7560
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-66-1211-11
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-10-4040
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-20-5535
FDA UDI
Class IIActive
uNion MAX UU202-03-02
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-82-1614-11
FDA UDI
Class IIActive
Momentum UU051-60-0090-L
FDA UDI
Class IIActive
Momentum UU051-60-0060-L
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-40-0030
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-40-0080
FDA UDI
Class IIActive
Momentum UU051-55-0035-L
FDA UDI
Class IIActive
Momentum UU062-82-0055
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-11-4036
FDA UDI
Class IIActive
Momentum MIS UU091-11-8540
FDA UDI
Class IIActive
Momentum MIS UU092-70-0101
FDA UDI
Class IIActive
uNion MAX UU201-21-4022
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-61-0080
FDA UDI
Class IIActive
uNion Cervical Plate System UM155-45-14
FDA UDI
Class IIActive
Momentum MIS UU091-60-0065
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.