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✓Medical device manufacturer · since 2010

Engineered in Ankara.
Built to a documented standard.

İnceler Medikal designs, manufactures and tests the Modus-F therapeutic massager, the only İnceler device available in the United States.

Modus-F therapeutic massager
ISO 13485Certified production
IEC 60601-1Electrical safety
2010
Founded in Ankara, Türkiye
30+
Countries supplied
1,500+
US clinics using Modus-F
1
Product offered in the US
What we do

Engineering, manufacturing and quality under one roof.

From the first drawing to the final test, Modus-F is designed, built and released by our own team in Ankara.

01

Engineering

In-house design of electronics, firmware, software and mechanical systems.

02

Manufacturing

Every unit assembled at our production facility in Ankara, Türkiye.

03

Quality

Production run under an ISO 13485-certified quality management system.

04

Compliance

US labeling, a single US product, and a clear line between US and international markets.

How every unit is made

Six steps from design to release.

Each Modus-F unit follows the same documented path before it leaves our facility.

STEP 01

Design

Design controls and documented specifications

STEP 02

Incoming inspection

Components checked against specification

STEP 03

Assembly

Built to controlled work instructions

STEP 04

Safety testing

Electrical safety and function tested on every unit

STEP 05

Labeling & UDI

US labeling and a unique device identifier

STEP 06

Release

Documented final release and traceability record

✓Available in the US Modus-F therapeutic massager
Our US product range

One device for the United States.

Our product range is different in every market. In the US, İnceler Medikal offers a single product.

Available in the US

Modus-F therapeutic massager

For temporary relief of minor muscle aches and pains and a temporary increase in local blood circulation.

Not available in the US

All other İnceler Medikal products

Products and uses on our international website are not cleared, approved or otherwise authorized by the U.S. FDA and are not offered for sale in the United States.

View Modus-F →
Standards

Built to recognized standards.

ISO 13485
Medical device quality management
IEC 60601-1
Basic safety of medical electrical equipment
IEC 60601-1-2
Electromagnetic compatibility
UDI
Unique device identifier on every unit
US labeling
English Instructions for Use with each device

Questions about Modus-F in the US?

Contact our authorized US distributor for sales, service and training.