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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
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LinkedIn
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Facebook
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Email
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Phone
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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 14 of 33
DeviceModel / ReferenceRegistriesClassStatus
Flux-C Cervical Interbody UU082-66-1412-11
FDA UDI
Class IIActive
Modified Instrument - LXH UU994-86-10
FDA UDI
Class IActive
uNion Cervical Plate System UM155-45-20
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-56-1614-08
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-10-4024
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-52-1412-06
FDA UDI
Class IIActive
Momentum UU051-02-5550
FDA UDI
Class IIActive
Momentum UU051-55-0090-L
FDA UDI
Class IIActive
uNion MAX UU201-22-4516
FDA UDI
Class IIActive
uNion Cervical Plate System UM150-40-20
FDA UDI
Class IIActive
Momentum UU051-00-5530
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1211-10
FDA UDI
Class IIActive
Momentum UU051-10-7545
FDA UDI
Class IIActive
Momentum UU051-02-4530
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-06-1614-07
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-60-0035
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-66-1412-08
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-06-1916-05
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-62-1916-09
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-20-5525
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-12-1916-11
FDA UDI
Class IIActive
uNion MAX UU201-22-4016
FDA UDI
Class IIActive
Momentum UU051-01-4530
FDA UDI
Class IIActive
Momentum MIS UU093-03-02
FDA UDI
Class IIActive
Momentum UU052-30-0200
FDA UDI
Class IIActive
Momentum MIS UU091-55-5100-L
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-62-1614-08
FDA UDI
Class IIActive
uNion MAX UU201-41-4522
FDA UDI
Class IIActive
uNion MAX UU201-02-0030
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-40-0140
FDA UDI
Class IIActive
uNion MAX UU202-10-22
FDA UDI
Class IIActive
Momentum UU052-30-0600
FDA UDI
Class IIActive
Momentum UU051-00-6555
FDA UDI
Class IIActive
Momentum UU062-84-0100
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU073-07-00
FDA UDI
Class IIActive
Momentum UU051-00-8535
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-00-1916-07
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-70-0002
FDA UDI
Class IIActive
uNion Cervical Plate System UM170-00-03
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-11-4020
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU073-01-05
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-10-3524
FDA UDI
Class IIActive
Momentum UU052-70-0010
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-00-1614-08
FDA UDI
Class IIActive
Momentum UU052-50-0080
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU081-00-1412-10
FDA UDI
Class IIActive
Momentum UU051-00-5550
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-21-5555
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-11-4040
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-40-5555
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.