Implantica highlights RefluxStop FDA approval
The device has strong European data from 1,800 patients and 38 publications across nine countries.
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Developer of implantable medical devices and eHealth platforms
implantica.comLast updated
In short: Implantica received FDA approval for RefluxStop and prepared U.S. launch with surgeon training.
The device has strong European data from 1,800 patients and 38 publications across nine countries.
FDA approval allows expansion of GERD treatment options for millions. The company thanks Nyelux for analysis.
The device aims to restore anti-reflux barrier function. Over 1,800 patients treated in Europe backed by extensive clinical research.
The company invites attendees to a session at the American Foregut Society Meeting discussing mechanisms, data, and global experience.
Medical technology company Implantica is receiving an injection of SEK 1.2 billion from the company's CEO and major shareholder Peter Forsell. At the same time, he wants a split in compensation...
Implantica AG announced that RefluxStop® received an enthusiastic welcome from surgeons and gastroenterologists at the 2026 annual meeting...
Implantica is launching RefluxStop in the US after a PMA approval that was based entirely on European trial data. A Medicare pass-through decision is expected...
Implantica's RefluxStop device for GORD treatment secured a European CE mark in 2018, with almost 1,800 patients treated to date.
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