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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 8 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-2460TTS
FDA UDI
Class IActive
Medfix MF-4645AS
FDA UDI
Class IActive
Medfix MF-8030
FDA UDI
Class IActive
Medfix MF-7466
FDA UDI
Class IActive
Medfix MF-20110TTB
FDA UDI
Class IActive
Medfix MF-1690TTS
FDA UDI
Class IActive
Medfix MF-1840TB
FDA UDI
Class IActive
Medfix MF-2360NS
FDA UDI
Class IActive
Medfix MFV-1000-INSERT
FDA UDI
Class IActive
Medfix MF676-7006B
FDA UDI
Class IActive
Medfix MF-9052
FDA UDI
Class IActive
Medfix MF-18110TS
FDA UDI
Class IActive
Medfix MF210-3400
FDA UDI
Class IActive
Medfix MF210-2400
FDA UDI
Class IActive
Medfix MF213-0001
FDA UDI
Class IActive
Medfix MF-9011
FDA UDI
Class IActive
Medfix MFP-2330NS
FDA UDI
Class IActive
Medfix MF750-3016
FDA UDI
Class IActive
Medfix MF-2360LLS
FDA UDI
Class IActive
Medfix MF-2630TS
FDA UDI
Class IActive
Medfix MF-18100TTS
FDA UDI
Class IActive
Medfix MF-2040TTB
FDA UDI
Class IActive
Medfix MFL-2355AS
FDA UDI
Class IActive
Medfix MF-9020
FDA UDI
Class IActive
Medfix MF260-1002
FDA UDI
Class IActive
Medfix MF-9045
FDA UDI
Class IActive
Medfix MF676-7004B
FDA UDI
Class IActive
Medfix MF283-2150-LID
FDA UDI
Class IActive
Medfix MF-2450TTB
FDA UDI
Class IActive
Medfix MF-5026
FDA UDI
Class IActive
Medfix MF-1660TS
FDA UDI
Class IActive
Medfix MF225-5817
FDA UDI
Class IActive
Medfix MF-1445SS
FDA UDI
Class IActive
Medfix MF137-7201B
FDA UDI
Class IActive
Medfix MF210-4002
FDA UDI
Class IActive
Medfix MF232-2352B
FDA UDI
Class IActive
Medfix MF-H4
FDA UDI
Class IActive
Medfix MF955-108
FDA UDI
Class IActive
Medfix MFP-2355NS
FDA UDI
Class IActive
Medfix MF-8714
FDA UDI
Class IActive
Medfix MF01878
FDA UDI
Class IActive
Medfix MF232-2482
FDA UDI
Class IActive
Medfix MF-8044
FDA UDI
Class IActive
Medfix MF110-1911-INSERT
FDA UDI
Class IActive
Medfix MF-2340LLS
FDA UDI
Class IActive
Medfix MF-8031
FDA UDI
Class IActive
Medfix MF200-0846-LID
FDA UDI
Class IActive
Medfix MF-7460
FDA UDI
Class IActive
Medfix MF750-3019
FDA UDI
Class IActive
Medfix MF240-7204T
FDA UDI
Class IActive

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