Implantica hosts a Capital Markets Day in Stockholm on September 9
The meeting outlines the U.S. launch strategy following FDA approval and features participating surgeons and patients.
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Developer of implantable medical devices and eHealth platforms
implantica.comLast updated
In short: Implantica received FDA premarket approval for its RefluxStop device and initiated plans for a commercial rollout in the United States.
The meeting outlines the U.S. launch strategy following FDA approval and features participating surgeons and patients.
The company secured Premarket Approval for RefluxStop, enabling a targeted commercial launch to treat GERD in the largest medical device market globally.
The e-InVivo platform enables remote monitoring and treatment adjustment of smart implants. RefluxStop demonstrated excellent outcomes in a five-year CE study.
The post educates on GERD symptoms and highlights RefluxStop as a minimally invasive procedure, pending FDA approval.
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...
The medtech company Implantica, active in the implant area, reports an operating result of minus 4.2 million euros (minus 4.5) for the...
The FDA granted premarket approval to RefluxStop, a non-drug implant device for treating gastroesophageal reflux disease (GERD), according to maker Implantica.
Implantica AG (OSTO:IMP A SDB) reports 66% revenue growth and outlines a strategic, step-by-step U.S. market entry following RefluxStop's FDA approval.
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