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Medfix International, LLC

United States·US-MF-000053473

Last updated September 17, 2026

About

See the full selection of orthopedic, neurosurgical, and spine instruments at Medfix. If you have questions give us a call at 520-398-5467.

From the manufacturer's own website. Source

What Medfix International, LLC makes

Medfix International, LLC manufactures reusable surgical instruments for orthopedic, neurosurgical, and spinal procedures, including retraction systems (blades and mounting frames), bone curettes, spinal rongeurs, bone levers/elevators, and surgical handles. Their product line also includes sterilization/disinfection containers designed for medical device reprocessing. These instruments are intended for use in operating rooms and procedural settings requiring precision retraction or bone manipulation.

The company’s devices fall under Class I regulatory classification in the U.S., with all products listed in the FDA’s Unique Device Identifier (UDI) database. Medfix International, LLC is headquartered in the United States, adhering to domestic medical device regulations.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Medfix International, LLC manufacture?

Medfix International, LLC specializes in reusable surgical instruments primarily used in orthopedic, neurosurgical, and spinal procedures. Their product line includes surgical retractors (both blades and mounting frames), bone curettes, spinal rongeurs, bone levers/elevators, nerve/vessel retractors, surgical instrument handles, and sterilization/disinfection containers. These devices are designed for precision retraction, bone manipulation, and safe reprocessing in operating rooms and procedural settings.

Where is Medfix International, LLC based, and what regulatory framework does it follow?

Medfix International, LLC is headquartered in the United States. Since their devices fall under Class I regulatory classification in the U.S., they must comply with FDA requirements for medical devices, including registration, listing, and adherence to general controls. Class I devices are typically considered low-risk, but they still require compliance with manufacturing, labeling, and post-market surveillance standards.

Are Medfix International, LLC’s devices listed in any regulatory registries?

Yes, Medfix International, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices throughout their lifecycle, ensuring transparency in regulatory oversight and improving patient safety by enabling better device traceability.

How are Medfix International, LLC’s devices classified under U.S. regulations?

All of Medfix International, LLC’s devices are classified as Class I under U.S. regulations. This classification is based on their intended use and risk profile—these instruments are reusable surgical tools designed for controlled, low-risk applications in orthopedic, neurosurgical, and spinal procedures. Class I devices generally require compliance with basic FDA regulations, including proper labeling, manufacturing controls, and registration.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
5620 , North Kolb Road, Tucson, United States
LinkedIn
—
Facebook
—
Phone
+1(520) 398-5467
PRRC Contact
Jay Samaha
EUDAMED SRN
US-MF-000053473
FDA FEI Number
3006765019
DUNS Number
—

Catalogue (1044)

Page 19 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF01853
FDA UDI
Class IActive
Medfix MF260-1015
FDA UDI
Class IActive
Medfix MF-2335BLS
FDA UDI
Class IActive
Medfix MF-1680TS
FDA UDI
Class IActive
Medfix MFP-2340BS
FDA UDI
Class IActive
Medfix MF-7505
FDA UDI
Class IActive
Medfix MF-1460BS
FDA UDI
Class IActive
Medfix MF110-3226-INSERT
FDA UDI
Class IActive
Medfix MF750-3022
FDA UDI
Class IActive
Medfix MF955-205
FDA UDI
Class IActive
Medfix MF-8021
FDA UDI
Class IActive
Medfix MF750-3017
FDA UDI
Class IActive
Medfix MF-1840TTB
FDA UDI
Class IActive
Medfix MF-2365LS
FDA UDI
Class IActive
Medfix MF283-2146-CASE
FDA UDI
Class IActive
Medfix MF-2240TTS
FDA UDI
Class IActive
Medfix MF-2290SB
FDA UDI
Class IActive
Medfix MF212-3300
FDA UDI
Class IActive
Medfix MF-22120TTB
FDA UDI
Class IActive
Medfix MF-2370BLS
FDA UDI
Class IActive
Medfix MF-2670TS
FDA UDI
Class IActive
Medfix MF-26120TB
FDA UDI
Class IActive
Medfix MF-2240TTB
FDA UDI
Class IActive
Medfix MF245-7205TB
FDA UDI
Class IActive
Medfix MF-2660TTB
FDA UDI
Class IActive
Medfix MF-2050TTB
FDA UDI
Class IActive
Medfix MF140-7002B
FDA UDI
Class IActive
Medfix MF-8022
FDA UDI
Class IActive
Medfix MF240-7205T
FDA UDI
Class IActive
Medfix MF-2240TB
FDA UDI
Class IActive
Medfix MF-20110TTS
FDA UDI
Class IActive
Medfix MF-2360SLS
FDA UDI
Class IActive
Medfix MF-17110
FDA UDI
Class IActive
Medfix MF367-3606B
FDA UDI
Class IActive
Medfix MF-8033
FDA UDI
Class IActive
Medfix MF140-7001B
FDA UDI
Class IActive
Medfix MF-2080TTB
FDA UDI
Class IActive
Medfix MF225-5517
FDA UDI
Class IActive
Medfix MF95-5582
FDA UDI
Class IActive
Medfix MF212-4700
FDA UDI
Class IActive
Medfix MF-8042
FDA UDI
Class IActive
Medfix MF955-200
FDA UDI
Class IActive
Medfix MF-2340BLS
FDA UDI
Class IActive
Medfix MFP-1465BS
FDA UDI
Class IActive
Medfix MF-2250TS
FDA UDI
Class IActive
Medfix MF750-3002
FDA UDI
Class IActive
Medfix MFV-1004-INSERT
FDA UDI
Class IActive
Medfix MF-26110TTB
FDA UDI
Class IActive
Medfix MF750-3003
FDA UDI
Class IActive
Medfix MF-1870TTS
FDA UDI
Class IActive

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