Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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
—
EUDAMED SRN
—
FDA FEI Number
3005532635
DUNS Number
—

Catalogue (1623)

Page 28 of 33
DeviceModel / ReferenceRegistriesClassStatus
Momentum UU051-00-8560
FDA UDI
Class IIActive
Solidity Vertebral Body Replacement UU042-02-01
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-56-1211-12
FDA UDI
Class IIActive
Momentum UU062-82-0065
FDA UDI
Class IIActive
uNion Cervical Plate System UM152-45-12
FDA UDI
Class IIActive
Momentum UU051-60-0035
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-70-1412-07
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1614-07
FDA UDI
Class IIActive
Momentum MIS UU092-50-0300
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1614-09
FDA UDI
Class IIActive
Momentum MIS UU091-20-9100
FDA UDI
Class IIActive
Momentum UU051-60-0100-L
FDA UDI
Class IIActive
Momentum MIS UU092-55-0302
FDA UDI
Class IIActive
uNion Cervical Plate System UM102-01-22
FDA UDI
Class IIActive
uNion Cervical Plate System UM154-40-18
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-56-1614-06
FDA UDI
Class IIActive
Momentum UU051-20-8090
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-11-0002
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-13-0410
FDA UDI
Class IIActive
Momentum UU052-62-0100
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-70-0101
FDA UDI
Class IIActive
uNion MAX UU201-03-0045
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-52-1211-09
FDA UDI
Class IIActive
uNion MAX UU201-01-0015
FDA UDI
Class IIActive
Momentum MIS UU091-60-0055
FDA UDI
Class IIActive
uNion MAX UU201-42-4512
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU073-06-01
FDA UDI
Class IIActive
Momentum UU052-10-0021
FDA UDI
Class IIActive
Momentum UU051-00-6535
FDA UDI
Class IIActive
Momentum UU052-11-0075
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-31-4026
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-70-5006
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-50-0030
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-20-4555
FDA UDI
Class IIActive
uNion Cervical Plate System UM191-01-05
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-62-1412-09
FDA UDI
Class IIActive
Momentum UU051-11-6560
FDA UDI
Class IIActive
Flux-C Cervical Interbody UU082-50-1211-06
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-31-4020
FDA UDI
Class IIActive
Momentum UU051-70-5506
FDA UDI
Class IIActive
Momentum UU051-26-0060
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU072-50-0048
FDA UDI
Class IIActive
Cortium Universal OCT Spinal Fixation System UU071-20-4535
FDA UDI
Class IIActive
Momentum UU051-10-5525
FDA UDI
Class IIActive
Momentum UU051-20-9070
FDA UDI
Class IIActive
uNion Cervical Plate System UM153-45-14
FDA UDI
Class IIActive
Momentum UU051-60-7300
FDA UDI
Class IIActive
Momentum UU052-60-0008
FDA UDI
Class IIActive
Momentum UU051-60-0030
FDA UDI
Class IIActive
Momentum UU051-70-0005
FDA UDI
Class IIActive

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.

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.