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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 3 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-MH2
FDA UDI
Class IActive
Medfix MF-1455BS
FDA UDI
Class IActive
Medfix MF225-5522
FDA UDI
Class IActive
Medfix MF-7471
FDA UDI
Class IActive
Medfix MF-23100FL
FDA UDI
Class IActive
Medfix MF-8046
FDA UDI
Class IActive
Medfix MF-0132
FDA UDI
Class IActive
Medfix MF10-10RH
FDA UDI
Class IActive
Medfix MF97-2857
FDA UDI
Class IActive
Medfix MF051-602
FDA UDI
Class IActive
Medfix MF676-7005B
FDA UDI
Class IActive
Medfix MF-7489
FDA UDI
Class IActive
Medfix MFL-2375AS
FDA UDI
Class IActive
Medfix MF-2030TTS
FDA UDI
Class IActive
Medfix MFV-1009L2-CASE
FDA UDI
Class IActive
Medfix MF750-3012
FDA UDI
Class IActive
Medfix MF-7510
FDA UDI
Class IActive
Medfix MF676-8501B
FDA UDI
Class IActive
Medfix MFP-2355SS
FDA UDI
Class IActive
Medfix MF-20100TTB
FDA UDI
Class IActive
Medfix MF-8017
FDA UDI
Class IActive
Medfix MFP-2370LS
FDA UDI
Class IActive
Medfix MF-8020
FDA UDI
Class IActive
Medfix MF232-2357B
FDA UDI
Class IActive
Medfix MF-0436
FDA UDI
Class IActive
Medfix MFV-1196-CASE
FDA UDI
Class IActive
Medfix MF-6702
FDA UDI
Class IActive
Medfix MF-0096
FDA UDI
Class IActive
Medfix MF-9041
FDA UDI
Class IActive
Medfix MF212-4800
FDA UDI
Class IActive
Medfix MF-1818
FDA UDI
Class IActive
Medfix MF110-3604-INSERT
FDA UDI
Class IActive
Medfix MF-2370SLS
FDA UDI
Class IActive
Medfix MF-8008
FDA UDI
Class IActive
Medfix MF-2080
FDA UDI
Class IActive
Medfix MF225-6405
FDA UDI
Class IActive
Medfix MF-MH3
FDA UDI
Class IActive
Medfix MF213-0002
FDA UDI
Class IActive
Medfix MF212-5200
FDA UDI
Class IActive
Medfix MF-2680TTS
FDA UDI
Class IActive
Medfix MFV-1011L-INSERT
FDA UDI
Class IActive
Medfix MF-8041
FDA UDI
Class IActive
Medfix MF750-3006
FDA UDI
Class IActive
Medfix MF249-7202T
FDA UDI
Class IActive
Medfix MF10-10RH-B
FDA UDI
Class IActive
Medfix MF-2375LS
FDA UDI
Class IActive
Medfix MF-23120FR
FDA UDI
Class IActive
Medfix MF-24120TTB
FDA UDI
Class IActive
Medfix MF218-001-INSERT
FDA UDI
Class IActive
Medfix MF-2230TTS
FDA UDI
Class IActive

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