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Our history

Medical innovation since 1999

MID (Medical Innovation Development) provides healthcare professionals with medical devices that meet demanding quality requirements. Innovation is part of the company culture, with active research and development projects focused on better answering clinical needs.

25+

Years of expertise

25

Countries

60+

Patents & trademarks

ISO

13485

MIDBAND™

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

Milestones in MID’s development

1999

MID SAS founded in Dardilly

2000

MIDBAND (ref. MID001)

2011

MIDSLEEVE (ref. MID160)

2013

MIDBAND (ref. MID100-M)

2014

MIDCAL (ref. MID180)

2015

MID-TUBE (ref. MID130)

2016

MID-SEW (ref. MID300)

2017

MID-TUBE (ref. MID136)

2018

MID-TUBE (ref. MID131)

2020

MID-VET (ref. MID300V)

2020

Metropolitan France distribution — SEJONG Medical monotrocart

2023

Korea FDA approval

2023

Taiwan FDA approval

2024

French distribution of the REACH SURGICAL stapling range

2026

Distribution of the BLUESAIL+ SURGICAL range

Our vocation

MID provides healthcare professionals with medical devices that meet demanding quality requirements.

Innovation is part of our culture. Active research and development projects help us answer clinical needs more precisely.

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.

Our international presence

In France, MID is one of the recognised players in medical devices dedicated to bariatric surgery. The company is present in more than twenty countries and a significant share of its activity is international.

DARDILLY · FRANCE

Made close to our teams

Design, development and quality are coordinated from the MID site near Lyon.

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

Our quality policy is based on listening to customers, regulatory compliance and continuous improvement.

01

Customer listening

Understand needs, validate proposed solutions and improve product performance and safety.

02

Compliance

Meet regulatory and normative requirements and mobilise the company around good practices.

03

ISO 13485

A quality management system for medical devices.