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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 2 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-2240BB
FDA UDI
Class IActive
Medfix MF-8027
FDA UDI
Class IActive
Medfix MF212-5100
FDA UDI
Class IActive
Medfix MF212-4600
FDA UDI
Class IActive
Medfix MFV-1010L-INSERT
FDA UDI
Class IActive
Medfix MF235-7203TB
FDA UDI
Class IActive
Medfix MF-27110
FDA UDI
Class IActive
Medfix MF-4022Ti
FDA UDI
Class IActive
Medfix MF260-1037
FDA UDI
Class IActive
Medfix MF-2470TTS
FDA UDI
Class IActive
Medfix MF-2013
FDA UDI
Class IActive
Medfix MF210-1100
FDA UDI
Class IActive
Medfix MF-0135
FDA UDI
Class IActive
Medfix MF-1890TB
FDA UDI
Class IActive
Medfix MF110-1865-INSERT
FDA UDI
Class IActive
Medfix MF-2430TTB
FDA UDI
Class IActive
Medfix MF229-5193
FDA UDI
Class IActive
Medfix MFP-1445SS
FDA UDI
Class IActive
Medfix MF-9013
FDA UDI
Class IActive
Medfix MF96-1562
FDA UDI
Class IActive
Medfix MF-18120TTS
FDA UDI
Class IActive
Medfix MFP-2355BS
FDA UDI
Class IActive
Medfix MF210-0500
FDA UDI
Class IActive
Medfix MF-1670TTB
FDA UDI
Class IActive
Medfix MF-7477
FDA UDI
Class IActive
Medfix MF213-0004
FDA UDI
Class IActive
Medfix MF-2330LS
FDA UDI
Class IActive
Medfix MF955-110
FDA UDI
Class IActive
Medfix MF-8040
FDA UDI
Class IActive
Medfix MF676-8504B
FDA UDI
Class IActive
Medfix MF-2340LS
FDA UDI
Class IActive
Medfix MF-8016
FDA UDI
Class IActive
Medfix MF-1660TTS
FDA UDI
Class IActive
Medfix MF750-3004
FDA UDI
Class IActive
Medfix MF955-204
FDA UDI
Class IActive
Medfix MF210-2300
FDA UDI
Class IActive
Medfix MF212-4000
FDA UDI
Class IActive
Medfix MF-18110TTS
FDA UDI
Class IActive
Medfix MF110-1928-INSERT
FDA UDI
Class IActive
Medfix MF-EC114
FDA UDI
Class IActive
Medfix MF-2450TTS
FDA UDI
Class IActive
Medfix MF-2230SB
FDA UDI
Class IActive
Medfix MF-8018
FDA UDI
Class IActive
Medfix MF-2335SLS
FDA UDI
Class IActive
Medfix MF229-5042
FDA UDI
Class IActive
Medfix MF-18100TTB
FDA UDI
Class IActive
Medfix MF337-1000
FDA UDI
Class IActive
Medfix MF212-4900
FDA UDI
Class IActive
Medfix MF-2340SS
FDA UDI
Class IActive
Medfix MF-6019Ti
FDA UDI
Class IActive

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