Medical technology company Implantica AG (Nasdaq First North Premier Growth Market: IMP A SDB) reported on Wednesday that it is ramping up production of its RefluxStop device with 10,000 units manufactured in preparation for a US launch, pending FDA premarket approval (PMA).
The company is building inventory, infrastructure and specialist teams to accelerate commercialisation and secure a rapid, scalable rollout in the US and other global markets once regulatory approvals are granted. By investing in early production, Implantica aims to avoid supply delays typically faced by medtech firms during initial market entry.
RefluxStop, already CE-marked in Europe, offers a novel treatment for gastroesophageal reflux disease (GERD), a condition affecting more than one billion people worldwide. Unlike traditional surgical methods that encircle the esophagus, the device restores the natural position of the lower esophageal sphincter without applying pressure, reducing common side effects such as swallowing difficulties.
Implantica is also advancing a broader pipeline based on its eHealth and wireless energising platforms, designed to enable remote-controlled implants and real-time health monitoring inside the body.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval