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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 15 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-2040
FDA UDI
Class IActive
Medfix MF-2350BS
FDA UDI
Class IActive
Medfix MF367-3603B
FDA UDI
Class IActive
Medfix MF-1680TB
FDA UDI
Class IActive
Medfix MF232-2612
FDA UDI
Class IActive
Medfix MF-2375BS
FDA UDI
Class IActive
Medfix MF-1880TTB
FDA UDI
Class IActive
Medfix MF-7503
FDA UDI
Class IActive
Medfix MF-EC84
FDA UDI
Class IActive
Medfix MF-0201
FDA UDI
Class IActive
Medfix MF225-6308
FDA UDI
Class IActive
Medfix MFP-2350LS
FDA UDI
Class IActive
Medfix MF96-1207
FDA UDI
Class IActive
Medfix MF245-7202TB
FDA UDI
Class IActive
Medfix MF750-3021
FDA UDI
Class IActive
Medfix MF-8048
FDA UDI
Class IActive
Medfix MF-1455SS
FDA UDI
Class IActive
Medfix MF-7479
FDA UDI
Class IActive
Medfix MF-1640TB
FDA UDI
Class IActive
Medfix MF-2280SB
FDA UDI
Class IActive
Medfix MF955-201
FDA UDI
Class IActive
Medfix MF-16120TS
FDA UDI
Class IActive
Medfix MF-0440
FDA UDI
Class IActive
Medfix MF-1880TB
FDA UDI
Class IActive
Medfix MF-22100TTS
FDA UDI
Class IActive
Medfix MF-2345BLS
FDA UDI
Class IActive
Medfix MFP-1455SS
FDA UDI
Class IActive
Medfix MF249-7203TCC
FDA UDI
Class IActive
Medfix MF750-3009
FDA UDI
Class IActive
Medfix MF-6016
FDA UDI
Class IActive
Medfix MF750-3020
FDA UDI
Class IActive
Medfix MF-27100
FDA UDI
Class IActive
Medfix MF-22110TTS
FDA UDI
Class IActive
Medfix MF-8038
FDA UDI
Class IActive
Medfix MF-7486
FDA UDI
Class IActive
Medfix MF-18120TB
FDA UDI
Class IActive
Medfix MF139-7003B
FDA UDI
Class IActive
Medfix MF-MH7
FDA UDI
Class IActive
Medfix MF-9003
FDA UDI
Class IActive
Medfix MF212-4400
FDA UDI
Class IActive
Medfix MF-1813
FDA UDI
Class IActive
Medfix MF-2730
FDA UDI
Class IActive
Medfix MF232-2477B
FDA UDI
Class IActive
Medfix MF-7022Ti
FDA UDI
Class IActive
Medfix MF-0102S
FDA UDI
Class IActive
Medfix MF750-3018
FDA UDI
Class IActive
Medfix MF212-4300
FDA UDI
Class IActive
Medfix MF212-3800
FDA UDI
Class IActive
Medfix MF-0130
FDA UDI
Class IActive
Medfix MF112-0165
FDA UDI
Class IActive

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