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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 18 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-1870TTB
FDA UDI
Class IActive
Medfix MF-8011
FDA UDI
Class IActive
Medfix MFP-2360BS
FDA UDI
Class IActive
Medfix MFP-2345SS
FDA UDI
Class IActive
Medfix MF367-3605B
FDA UDI
Class IActive
Medfix MF-2370SS
FDA UDI
Class IActive
Medfix MF-7474
FDA UDI
Class IActive
Medfix MF-2280TTS
FDA UDI
Class IActive
Medfix MF-2365AS
FDA UDI
Class IActive
Medfix MF-7497
FDA UDI
Class IActive
Medfix MF-26110TS
FDA UDI
Class IActive
Medfix MF212-4500
FDA UDI
Class IActive
Medfix MF-7499
FDA UDI
Class IActive
Medfix MF-2335BS
FDA UDI
Class IActive
Medfix MF249-7201TCC
FDA UDI
Class IActive
Medfix MF750-3026
FDA UDI
Class IActive
Medfix MF-2050
FDA UDI
Class IActive
Medfix MF-7491
FDA UDI
Class IActive
Medfix MF-2370NS
FDA UDI
Class IActive
Medfix MF-9015
FDA UDI
Class IActive
Medfix MF249-7202TCC
FDA UDI
Class IActive
Medfix MF-2350BLS
FDA UDI
Class IActive
Medfix MF-4635AS
FDA UDI
Class IActive
Medfix MF-7461S
FDA UDI
Class IActive
Medfix MF-2375NS
FDA UDI
Class IActive
Medfix MF-2240TS
FDA UDI
Class IActive
Medfix MFP-2330SS
FDA UDI
Class IActive
Medfix MF-9040
FDA UDI
Class IActive
Medfix MF137-7101B
FDA UDI
Class IActive
Medfix MF-7490S
FDA UDI
Class IActive
Medfix MF232-9052
FDA UDI
Class IActive
Medfix MF-2640TB
FDA UDI
Class IActive
Medfix MF112-0152
FDA UDI
Class IActive
Medfix MF213-1005
FDA UDI
Class IActive
Medfix MF93-2472
FDA UDI
Class IActive
Medfix MF-2440TTS
FDA UDI
Class IActive
Medfix MF-23120FL
FDA UDI
Class IActive
Medfix MF-1650TB
FDA UDI
Class IActive
Medfix MF249-7203T
FDA UDI
Class IActive
Medfix MF-4665AS
FDA UDI
Class IActive
Medfix MF-22100SB
FDA UDI
Class IActive
Medfix MF-9001
FDA UDI
Class IActive
Medfix MF-20120TTB
FDA UDI
Class IActive
Medfix MF-2375LLS
FDA UDI
Class IActive
Medfix MF-8036
FDA UDI
Class IActive
Medfix MF-1440BS
FDA UDI
Class IActive
Medfix MF212-3700
FDA UDI
Class IActive
Medfix MF-2375AS
FDA UDI
Class IActive
Medfix MF-6701
FDA UDI
Class IActive
Medfix MF-1470SS
FDA UDI
Class IActive

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