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Our history

25 years of medical innovation for surgeons

Founded in 1999 in Dardilly near Lyon, MID has developed unique expertise in the design and manufacture of medical-grade silicone devices for bariatric surgery and beyond. ISO 13485 certified and present in 25 countries, MID co-develops solutions with surgeons.

25+

Years of expertise

25

Countries

60+

Patents & trademarks

ISO

13485
MID medical device manufacturing in France

MIDBAND™

Low-pressure adjustable gastric band, made in France and designed for qualified bariatric surgeons.

Technical sheet

A history built around clinical needs

1999

MID SAS founded in Dardilly, Lyon

Founded in 1999 in Dardilly near Lyon, MID has developed unique expertise in the design and manufacture of medical-grade silicone devices for bariatric surgery and beyond. ISO 13485 certified and present in 25 countries, MID co-develops solutions with surgeons.

~2002

MIDBAND™ launched

~2008

ISO 13485 certification

~2012

MIDSLEEVE™ and international expansion

~2018

MID-VET™ for equine surgery

2023

REACH SURGICAL and SEJONG partnerships

2024

MID-CARE launched

Timeline dates marked with ~ require client validation.

Our mission

We design, develop, manufacture and market solutions for healthcare professionals, meeting demanding quality requirements.

Our collaborations

We work with recognised scientific and clinical leaders. Our R&D department applies Validation and Verification procedures from the idea to industrialisation and commercialisation.

We hold more than 60 patents and 15 trademarks.

The principles that guide MID

01

Adaptability

Innovation is part of our culture, with an active R&D pipeline focused on professional healthcare needs.

02

Proximity

Co-development with clinical experts, from the idea to industrialisation.

03

Expertise

Design in Dardilly using 3D modelling, numerical simulation and 3D printing.

04

Reliability

ISO 13485, CE MDR, Taiwan, Australia and UK quality requirements with full traceability.

Quality is designed into every stage

01

ISO 13485

Medical device quality management system.

02

CE · MDR 2017/745

European regulatory marking.

03

TFDA · TGA · MHRA

International market authorisations listed in the brief.