Maestro Logistics, LLC

FDA Device Registration & Listing · Austin, TX, US · Registration 3014129047

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
3014129047
FEI Number
3019827409
Entity Name
Maestro Logistics, LLC
City/State/Country
Austin, TX, US
Establishment Address
11000 N Mopac Expy, Suite 250, Austin, TX 78759, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Maestro Logistics (Owner Number: 10056045)
Owner / Operator Contact Address
11000 N Mopac Expy, Suite 250, Austin, TX 78759, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

OsteoCentric Spine MIS Pedicle Fastener System OsteoCentric Technologies Headless Compression System OsteoCentric Extremities Headless Compression System OsteoCentric Trauma Headless Compression System OsteoCentric Trauma Bone Fastener OsteoCentric Integrity SI fusion System OsteoCentric Technologies Cannulated System OsteoCentric Trauma Cancellous Bone Screw Fastener System OsteoCentric Trauma Cannulated Bone Screw Fastener System OsteoCentric Integrity SI fusion System OsteoCentric Bone Plate and screw system (Line Extension for the Clavicle Plate) OsteoCentric Trauma Bone Screw OsteoCentric Technologies Integrated Hip Fastener System ACL Fastener system Dental Implant System OsteoCentric Trauma Schanz Screw OsteoCentric Technologies Cannulated Fastener System OsteoCentric Hip Fastener System OsteoCentric Trauma K-Wire and Pins OsteoCentric Technologies K-Wire and Pins

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 2022-12-28
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2022-12-28
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2019-03-27
OUR Sacroiliac Joint Fixation Orthopedic Class 2 888.3040 2021-12-28
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2021-12-28
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2021-12-28
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2019-03-27
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2019-03-27
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2019-03-27
OUR Sacroiliac Joint Fixation Orthopedic Class 2 888.3040 2022-12-28
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2025-05-12
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2025-05-12
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2025-05-12
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2019-03-27
JDO Device, Fixation, Proximal Femoral, Implant Orthopedic Class 2 888.3030 2021-12-28
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2021-12-28
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2024-11-14
DZE Implant, Endosseous, Root-Form Dental Class 2 872.3640 2024-11-14
NHA Abutment, Implant, Dental, Endosseous Dental Class 2 872.3630 2024-11-14
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2019-03-27
HWC Screw, Fixation, Bone Orthopedic Class 2 888.3040 2021-12-28
HTN Washer, Bolt Nut Orthopedic Class 2 888.3030 2021-12-28
JDO Device, Fixation, Proximal Femoral, Implant Orthopedic Class 2 888.3030 2024-11-14
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2024-11-14
JDW Pin, Fixation, Threaded Orthopedic Class 2 888.3040 2021-12-28
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2021-12-28

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Maestro Logistics
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 3014129047. Last updated year: 2026. Please use registration number 3014129047 when referencing this establishment in official correspondence.
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