MET ONE TECHNOLOGIES, LLC

FDA Device Registration & Listing · El Paso, TX, US · Registration 3012994232

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
3012994232
FEI Number
3012994232
Entity Name
MET ONE TECHNOLOGIES, LLC
City/State/Country
El Paso, TX, US
Establishment Address
4519 Osborne Dr., Suite C, El Paso, TX 79922, US
Establishment Type(s)
Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MET ONE TECHNOLOGIES, LLC (Owner Number: 10052587)
Owner / Operator Contact Address
4519 Osborne Dr., Suite C, El Paso, TX 79922, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K160699
PMA Number
N/A

All Registered Proprietary Names

AUDERE C CERVICAL KODIAK PL & TL XULTAN 5.5 PEDICLE SCREW SYSTEM CZAR CERVICAL PLATE KODIAK C CERVICAL AUDERE PL & TL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MQP Spinal Vertebral Body Replacement Device Orthopedic Class 2 888.3060 2017-10-27
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2017-10-27
NKG Posterior Cervical Screw System Orthopedic Class 2 888.3075 2026-02-02
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2023-06-05
NKB Thoracolumbosacral Pedicle Screw System Orthopedic Class 2 888.3070 2017-10-27
KWQ Appliance, Fixation, Spinal Intervertebral Body Orthopedic Class 2 888.3060 2019-01-23
MQP Spinal Vertebral Body Replacement Device Orthopedic Class 2 888.3060 2023-02-17
ODP Intervertebral Fusion Device With Bone Graft, Cervical Orthopedic Class 2 888.3080 2023-02-17
MAX Intervertebral Fusion Device With Bone Graft, Lumbar Orthopedic Class 2 888.3080 2016-08-22

Official Correspondent

Liberato Aguilar

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MET ONE TECHNOLOGIES, LLC
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
K041888 Signus Medizintechnik GmbH CURVED PEEK TETRIS SPINAL IMPLANT 2004-08-10
K211892 Arftx Medical, LLC ArtFx Corpectomy Cages (Espinax and Distractania Corpectomy Cages) 2022-10-06
K070082 Vertebration,Inc XY COR SPINAL IMPLANT FOR MINIMAL INVASIVE SPINAL SURGERY 2007-04-20
K051027 Surgicraft , Ltd. STALIF TT 2005-06-29
K142269 Reliance Medical Systems, LLC Reliance Cervical IBF System 2015-06-09

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 3012994232. Last updated year: 2026. Please use registration number 3012994232 when referencing this establishment in official correspondence.
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