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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 13 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-0108
FDA UDI
Class IActive
Medfix MF-2375FL
FDA UDI
Class IActive
Medfix MF-0105S
FDA UDI
Class IActive
Medfix MF-1650TTS
FDA UDI
Class IActive
Medfix MF-1475BS
FDA UDI
Class IActive
Medfix MF95-2722
FDA UDI
Class IActive
Medfix MF249-7106T
FDA UDI
Class IActive
Medfix MF-2360LS
FDA UDI
Class IActive
Medfix MF283-2149-CASE
FDA UDI
Class IActive
Medfix MF-7165
FDA UDI
Class IActive
Medfix MF-2345NS
FDA UDI
Class IActive
Medfix MF225-5822
FDA UDI
Class IActive
Medfix MF306-3407
FDA UDI
Class IActive
Medfix MF226-5737
FDA UDI
Class IActive
Medfix MF-2650TB
FDA UDI
Class IActive
Medfix MF235-7204TB
FDA UDI
Class IActive
Medfix MF750-3013
FDA UDI
Class IActive
Medfix MF-2070TTS
FDA UDI
Class IActive
Medfix MF-2250SB
FDA UDI
Class IActive
Medfix MFL-23100AS
FDA UDI
Class IActive
Medfix MF-7496
FDA UDI
Class IActive
Medfix MF225-5972
FDA UDI
Class IActive
Medfix MF-8024Ti
FDA UDI
Class IActive
Medfix MF249-7204T
FDA UDI
Class IActive
Medfix MF-2690TS
FDA UDI
Class IActive
Medfix MF-26100TB
FDA UDI
Class IActive
Medfix MF-2060TTS
FDA UDI
Class IActive
Medfix MF-1460SS
FDA UDI
Class IActive
Medfix MF210-2100
FDA UDI
Class IActive
Medfix MFV-1010-INSERT-18L
FDA UDI
Class IActive
Medfix MF93-5302
FDA UDI
Class IActive
Medfix MFP-1435SS
FDA UDI
Class IActive
Medfix MF-1860TTB
FDA UDI
Class IActive
Medfix MF-2280TS
FDA UDI
Class IActive
Medfix MF-1435BS
FDA UDI
Class IActive
Medfix MF-8024
FDA UDI
Class IActive
Medfix MF-1670TS
FDA UDI
Class IActive
Medfix MF-9009
FDA UDI
Class IActive
Medfix MF-7001
FDA UDI
Class IIActive
Medfix MFP-1435BS
FDA UDI
Class IActive
Medfix MF367-2606B
FDA UDI
Class IActive
Medfix MF-1008Ti
FDA UDI
Class IActive
Medfix MF240-7202T
FDA UDI
Class IActive
Medfix MF-26120TTS
FDA UDI
Class IActive
Medfix MF-0437
FDA UDI
Class IActive
Medfix MFP-1440BS
FDA UDI
Class IActive
Medfix MF-20100TTS
FDA UDI
Class IActive
Medfix MF-2330BS
FDA UDI
Class IActive
Medfix MF106-5752
FDA UDI
Class IActive
Medfix MF-2060TTB
FDA UDI
Class IActive

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