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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 20 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF137-7002B
FDA UDI
Class IActive
Medfix MF-2335NS
FDA UDI
Class IActive
Medfix MF-7488
FDA UDI
Class IActive
Medfix MF225-5832
FDA UDI
Class IActive
Medfix MF-1630TS
FDA UDI
Class IActive
Medfix MF-0434
FDA UDI
Class IActive
Medfix MF249-7102TCC
FDA UDI
Class IActive
Medfix MF-7475
FDA UDI
Class IActive
Medfix MF235-7204T
FDA UDI
Class IActive
Medfix MF213-1003
FDA UDI
Class IActive
Medfix MF-1640TS
FDA UDI
Class IActive
Medfix MF-2335LLS
FDA UDI
Class IActive
Medfix MF676-8502B
FDA UDI
Class IActive
Medfix MF-24110TTS
FDA UDI
Class IActive
Medfix MF-2470TTB
FDA UDI
Class IActive
Medfix MF232-2487
FDA UDI
Class IActive
Medfix MF-1670TB
FDA UDI
Class IActive
Medfix MF367-2603B
FDA UDI
Class IActive
Medfix MF-2070TTB
FDA UDI
Class IActive
Medfix MF283-2145-LID
FDA UDI
Class IActive
Medfix MF212-3200
FDA UDI
Class IActive
Medfix MF-2355FL
FDA UDI
Class IActive
Medfix MF-23120AS
FDA UDI
Class IActive
Medfix MF-1880TTS
FDA UDI
Class IActive
Medfix MF210-3500
FDA UDI
Class IActive
Medfix MF-H7
FDA UDI
Class IActive
Medfix MF01854
FDA UDI
Class IActive
Medfix MF-1640TTS
FDA UDI
Class IActive
Medfix MF-0098
FDA UDI
Class IActive
Medfix MF-MH9
FDA UDI
Class IActive
Medfix MF-EC83
FDA UDI
Class IActive
Medfix MF-1790
FDA UDI
Class IActive
Medfix MF-2630TTS
FDA UDI
Class IActive
Medfix MF-1860TTS
FDA UDI
Class IActive
Medfix MF-MH6
FDA UDI
Class IActive
Medfix MFP-2365BS
FDA UDI
Class IActive
Medfix MF303-3402
FDA UDI
Class IActive
Medfix MF-2490TTB
FDA UDI
Class IActive
Medfix MFP-2350BS
FDA UDI
Class IActive
Medfix MF-2355BS
FDA UDI
Class IActive
Medfix MF-1435SS
FDA UDI
Class IActive
Medfix MFP-2375BS
FDA UDI
Class IActive
Medfix MF-1770
FDA UDI
Class IActive
Medfix MF-1860TS
FDA UDI
Class IActive
Medfix MF-1780
FDA UDI
Class IActive
Medfix MF212-4100
FDA UDI
Class IActive
Medfix MF-2250BB
FDA UDI
Class IActive
Medfix MF249-7204TCC
FDA UDI
Class IActive
Medfix MF-2660TB
FDA UDI
Class IActive
Medfix MF267-2605B
FDA UDI
Class IActive

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