ULRICH MEDICAL USA, INC.

FDA Device Registration & Listing · Plano, TX, US · Registration 3005823819

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005823819
FEI Number
3005532635
Entity Name
ULRICH MEDICAL USA, INC.
City/State/Country
Plano, TX, US
Establishment Address
3700 East Plano Parkway, Suite 200, Plano, TX 75074, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
ULRICH MEDICAL USA, INC. (Owner Number: 9062154)
Owner / Operator Contact Address
3700 East Plano Parkway, Suite 200, --, Plano, TX 75074, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Momentum Posterior Spinal Fixation System Solidity Vertebral Body Replacement uNion MAX drill V-Steady Cement uCerv Flux C hyperlordotic Control Handle Momentum MIS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NKB Thoracolumbosacral Pedicle Screw System Orthopedic Class 2 888.3070 2019-10-07
MQP Spinal Vertebral Body Replacement Device Orthopedic Class 2 888.3060 2018-12-06
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2026-04-13
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2022-08-25
KWQ Appliance, Fixation, Spinal Intervertebral Body Orthopedic Class 2 888.3060 2024-07-12
HWX Tap, Bone Orthopedic Class 1 888.4540 2024-07-12
NKB Thoracolumbosacral Pedicle Screw System Orthopedic Class 2 888.3070 2024-07-12
PML Bone Cement, Posterior Screw Augmentation Orthopedic Class 2 888.3027 2024-07-12
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2025-12-01
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2020-11-02
LXH Orthopedic Manual Surgical Instrument Orthopedic Class 1 888.4540 2023-07-13
NKB Thoracolumbosacral Pedicle Screw System Orthopedic Class 2 888.3070 2023-06-13

Official Correspondent

Eric Gibbs

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ULRICH MEDICAL USA, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K163363 Surgtech, Inc. SurgTech Thoracolumbosacral (TLS) Posterior Fixation System 2017-04-05
K252461 Spinal Resources, Inc. Swedge™ Pedicle Screw Fixation System Bezier Rod 2026-01-13
K140696 Pioneer Surgical Technology, Inc. STREAMLINE TL SPINAL FIXATION SYSTEM 2014-04-10
K141398 Medicrea International SA PASS LP SPINAL SYSTEM 2015-01-09
K160980 Spineology, Inc. Threshold Pedicular Fixation System, Palisade Pedicular Fixation System 2016-05-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2013 Synthes USA HQ, Inc. 2
MIRS for MATRIX Spine System. Minimally Invasive Reduction Screw (MIRS) for percutaneous instrumentation of the thoracolumbar spine. The Synthes USS are non-cervial spinal fixation devices intended for posterior pedicle screw fixation (T1-S2/ilium), posterior hook fixation (T1-L5), or anterolateral fixation (T8-L5).
Z-0004-2008 Abbott Spine 2
PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stablization system, Part Number 1156-50.
Z-0005-2008 Abbott Spine 2
PathFinder Bone Drill-Awl-Tap, a part of the PathFinder spinal stabilization system, Part Number 1156-60.
Z-0020-06 Pioneer Surgical Technology 2
Pioneer Surgical brand Quantum Spinal Rod System Polyaxial Screw, length 45 mm; Catalog number 10-575-PA-45.
Z-0021-06 Pioneer Surgical Technology 2
Pioneer Surgical brand Quantum Spinal Rod System Polyaxial Screw, length 40 mm; Catalog number 10-575-PA-40.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005823819. Last updated year: 2026. Please use registration number 3005823819 when referencing this establishment in official correspondence.
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