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SuperSeton

The startup develops medical healthcare products specifically designed for patients with anal fistulae, utilizing disposable applicators for manual application. Their products minimize irritation and discomfort, enhancing patient mobility and overall quality of life.

Amsterdam, The NetherlandsFounded 20175100+ followers
Updated 18 months ago

Funding

$460K raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.

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Funding rounds are not available yet.

Founders

Product

Problem

Traditional setons used for perianal fistula drainage often employ a knot, which can cause pain, irritation, and discomfort for patients, limiting their mobility and potentially leading to complications and increased healthcare costs.

Solution

SuperSeton offers a knotless seton drainage solution designed to minimize irritation and enhance patient comfort. The device features a smooth, flexible, and secure double-wedged closure that can be manually applied in seconds using a patented disposable applicator. This innovative design integrates seamlessly with established practices, improving the efficiency of fistula treatment while significantly increasing patients' mobility and overall quality of life. The SuperSeton is manufactured from high-quality medical-grade materials and has been clinically approved and tested to ensure it can withstand forces exerted during use.

Target Audience

The primary target audience includes surgeons, doctors, and healthcare institutions specializing in the treatment of perianal fistulas.

Features

  • Knotless design to reduce pain and irritation
  • Smooth, 360º round construction for enhanced comfort
  • Secure and flexible double-wedged closure mechanism
  • Patented disposable applicator for quick and easy manual application
  • High-quality, medical-grade materials
  • Clinically approved and tested for safety and reliability
  • Sterile medical device
  • Compliant with directive 93/42/EEC on medical devices and ISO 13485:2016 certified
This profile is AI-generated and may contain inaccuracies.