Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 5 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-7465
FDA UDI
Class IActive
Medfix MF-2260SB
FDA UDI
Class IActive
Medfix MF-9046
FDA UDI
Class IActive
Medfix MF-4685AS
FDA UDI
Class IActive
Medfix MF225-5967
FDA UDI
Class IActive
Medfix MF-7491S
FDA UDI
Class IActive
Medfix MF676-8503
FDA UDI
Class IActive
Medfix MF112-0153
FDA UDI
Class IActive
Medfix MF-2750
FDA UDI
Class IActive
Medfix MF210-1400
FDA UDI
Class IActive
Medfix MF249-7205TCC
FDA UDI
Class IActive
Medfix MF-8032
FDA UDI
Class IActive
Medfix MF240-7206T
FDA UDI
Class IActive
Medfix MFP-2335SS
FDA UDI
Class IActive
Medfix MF-7467
FDA UDI
Class IActive
Medfix MF-23100AS
FDA UDI
Class IActive
Medfix MF-1850TTS
FDA UDI
Class IActive
Medfix MF-2345SS
FDA UDI
Class IActive
Medfix MF235-7206TB
FDA UDI
Class IActive
Medfix MF955-106
FDA UDI
Class IActive
Medfix MFP-1440SS
FDA UDI
Class IActive
Medfix MF-2365FR
FDA UDI
Class IActive
Medfix MF110-3135
FDA UDI
Class IActive
Medfix MF283-2145-CASE
FDA UDI
Class IActive
Medfix MF212-3900
FDA UDI
Class IActive
Medfix MF138-7002B
FDA UDI
Class IActive
Medfix MF-2270BB
FDA UDI
Class IActive
Medfix MF-9005
FDA UDI
Class IActive
Medfix MF249-7103TCC
FDA UDI
Class IActive
Medfix MF-2070
FDA UDI
Class IActive
Medfix MF249-7101TCC
FDA UDI
Class IActive
Medfix MF225-5897
FDA UDI
Class IActive
Medfix MF-3018
FDA UDI
Class IActive
Medfix MF-2370LLS
FDA UDI
Class IActive
Medfix MF-1450BS
FDA UDI
Class IActive
Medfix MF-22120TS
FDA UDI
Class IActive
Medfix MF212-3500
FDA UDI
Class IActive
Medfix MF-2660TS
FDA UDI
Class IActive
Medfix MF-2385FR
FDA UDI
Class IActive
Medfix MF110-1866-INSERT
FDA UDI
Class IActive
Medfix MFP-2370SS
FDA UDI
Class IActive
Medfix MF676-7003B
FDA UDI
Class IActive
Medfix MF955-206
FDA UDI
Class IActive
Medfix MF676-8505B
FDA UDI
Class IActive
Medfix MF249-7201T
FDA UDI
Class IActive
Medfix MF-2330LLS
FDA UDI
Class IActive
Medfix MF-EC113
FDA UDI
Class IActive
Medfix MFP-1475SS
FDA UDI
Class IActive
Medfix MF-9017
FDA UDI
Class IActive
Medfix MF-1860TB
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.