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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 11 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-2230TTB
FDA UDI
Class IActive
Medfix MFP-2360NS
FDA UDI
Class IActive
Medfix MF01860
FDA UDI
Class IActive
Medfix MF-9047
FDA UDI
Class IActive
Medfix MF676-8501
FDA UDI
Class IActive
Medfix MF232-7007
FDA UDI
Class IActive
Medfix MF210-1300
FDA UDI
Class IActive
Medfix MF245-7203TB
FDA UDI
Class IActive
Medfix MF-0438
FDA UDI
Class IActive
Medfix MF-7473
FDA UDI
Class IActive
Medfix MF-1475SS
FDA UDI
Class IActive
Medfix MF-2360BLS
FDA UDI
Class IActive
Medfix MFP-2330BS
FDA UDI
Class IActive
Medfix MF-EC81
FDA UDI
Class IActive
Medfix MF-EC112
FDA UDI
Class IActive
Medfix MF235-7202TB
FDA UDI
Class IActive
Medfix MF-7494
FDA UDI
Class IActive
Medfix MF212-5300
FDA UDI
Class IActive
Medfix MF-2335SS
FDA UDI
Class IActive
Medfix MF306-4302
FDA UDI
Class IActive
Medfix MF213-1004
FDA UDI
Class IActive
Medfix MF110-3136
FDA UDI
Class IActive
Medfix MF-2630TTB
FDA UDI
Class IActive
Medfix MF-1830TTS
FDA UDI
Class IActive
Medfix MF-18110TB
FDA UDI
Class IActive
Medfix MF210-0100
FDA UDI
Class IActive
Medfix MF-16100TTS
FDA UDI
Class IActive
Medfix MFP-1445BS
FDA UDI
Class IActive
Medfix MF955-112
FDA UDI
Class IActive
Medfix MF-8029
FDA UDI
Class IActive
Medfix MF-2680TS
FDA UDI
Class IActive
Medfix MFP-2345BS
FDA UDI
Class IActive
Medfix MF-7511
FDA UDI
Class IActive
Medfix MF-9039
FDA UDI
Class IActive
Medfix MF-4675AS
FDA UDI
Class IActive
Medfix MF-EC115
FDA UDI
Class IActive
Medfix MF212-5000
FDA UDI
Class IActive
Medfix MF-9042
FDA UDI
Class IActive
Medfix MF750-3024
FDA UDI
Class IActive
Medfix MF-9022
FDA UDI
Class IActive
Medfix MF-2365SS
FDA UDI
Class IActive
Medfix MF267-3604B
FDA UDI
Class IActive
Medfix MF-2460TTB
FDA UDI
Class IActive
Medfix MF-2013Ti
FDA UDI
Class IActive
Medfix MF213-1001
FDA UDI
Class IActive
Medfix MF-2355NS
FDA UDI
Class IActive
Medfix MF-1890TTS
FDA UDI
Class IActive
Medfix MF-9000
FDA UDI
Class IActive
Medfix MF-1890TTB
FDA UDI
Class IActive
Medfix MF-7464
FDA UDI
Class IActive

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