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Cosm

Cosm offers Gynethotics™, the first personalized pessaries for pelvic floor disorders, using a clinician‑driven software platform and 3D printing to create patient‑specific devices. The solution eliminates trial‑and‑error fitting, improves comfort and adherence, and provides cloud‑based tracking of outcomes, all under Health Canada licensing and FDA clearance.

Toronto, CanadaFounded 2017305K+ followers
Updated 2 months ago

Funding

$5.1M 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.

Funding rounds are not available yet.

Founders

Product

Problem

Many women with pelvic floor disorders such as prolapse and urinary incontinence struggle to find a pessary that fits comfortably, leading to high discontinuation rates, discomfort, and limited effectiveness of conservative treatment.

Solution

Cosm provides personalized pessaries—Gynethotics™—that are custom‑designed for each patient using 3D printing and proprietary software. Clinicians input patient‑specific anatomical data, and the platform generates a digital model that is printed to exact dimensions, ensuring optimal fit and comfort. The solution eliminates the trial‑and‑error fitting process, reduces adverse events, and improves adherence to non‑surgical management. Data from each device can be tracked through Cosm’s digital gynecology software, enabling clinicians to monitor outcomes and adjust designs over time. The system is Health Canada licensed and FDA cleared, supporting safe deployment in clinical settings.

Target Audience

Primary customers are gynecologists, urogynecologists, and pelvic health clinicians who prescribe pessaries for prolapse and incontinence management.

Features

  • Patient‑specific 3D‑printed pessary designs generated from clinician‑entered digital measurements
  • Integrated software workflow that automates design optimization and printing instructions
  • Compatibility with standard 3D printing materials approved for vaginal use
  • Cloud‑based tracking of device fit, usage, and patient outcomes for continuous care improvement
  • Regulatory compliance (Health Canada license, FDA clearance) ensuring safety and quality
This profile is AI-generated and may contain inaccuracies.