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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 10 of 21
DeviceModel / ReferenceRegistriesClassStatus
Medfix MF-0088
FDA UDI
Class IActive
Medfix MF955-109
FDA UDI
Class IActive
Medfix MF260-1008
FDA UDI
Class IActive
Medfix MF-2430TTS
FDA UDI
Class IActive
Medfix MFP-2360SS
FDA UDI
Class IActive
Medfix MF955-207-INSERT
FDA UDI
Class IActive
Medfix MF-1890TS
FDA UDI
Class IActive
Medfix MF93-2432
FDA UDI
Class IActive
Medfix MF-0117
FDA UDI
Class IActive
Medfix MF-2290TB
FDA UDI
Class IActive
Medfix MF-MH8
FDA UDI
Class IActive
Medfix MF955-111
FDA UDI
Class IActive
Medfix MFP-1465SS
FDA UDI
Class IActive
Medfix MF232-9057
FDA UDI
Class IActive
Medfix MF-H8
FDA UDI
Class IActive
Medfix MF-7484
FDA UDI
Class IActive
Medfix MF137-7001B
FDA UDI
Class IActive
Medfix MF213-1002
FDA UDI
Class IActive
Medfix MF-2375SS
FDA UDI
Class IActive
Medfix MF-2640TTB
FDA UDI
Class IActive
Medfix MF-2050TTS
FDA UDI
Class IActive
Medfix MF110-1897-INSERT
FDA UDI
Class IActive
Medfix MF-2090TTS
FDA UDI
Class IActive
Medfix MF-7480
FDA UDI
Class IActive
Medfix MF110-1815-INSERT
FDA UDI
Class IActive
Medfix MFP-2365LS
FDA UDI
Class IActive
Medfix MFP-2335BS
FDA UDI
Class IActive
Medfix MF96-2207
FDA UDI
Class IActive
Medfix MF-2330BLS
FDA UDI
Class IActive
Medfix MF-2270SB
FDA UDI
Class IActive
Medfix MF-9006
FDA UDI
Class IActive
Medfix MF232-9062
FDA UDI
Class IActive
Medfix MF-4655AS
FDA UDI
Class IActive
Medfix MF210-1200
FDA UDI
Class IActive
Medfix MF-2290TTB
FDA UDI
Class IActive
Medfix MF110-3212-INSERT
FDA UDI
Class IActive
Medfix MF-8004
FDA UDI
Class IActive
Medfix MF-6704
FDA UDI
Class IActive
Medfix MFP-2365NS
FDA UDI
Class IActive
Medfix MF249-7101T
FDA UDI
Class IActive
Medfix MF-2670TTB
FDA UDI
Class IActive
Medfix MF232-2607B
FDA UDI
Class IActive
Medfix MFL-2385AS
FDA UDI
Class IActive
Medfix MF-7485
FDA UDI
Class IActive
Medfix MF-9010
FDA UDI
Class IActive
Medfix MF212-5400
FDA UDI
Class IActive
Medfix MF-16110TS
FDA UDI
Class IActive
Medfix MFP-1475BS
FDA UDI
Class IActive
Medfix MF-2250TB
FDA UDI
Class IActive
Medfix MF-7493
FDA UDI
Class IActive

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