Rivermark Medical


Rivermark Medical is dedicated to redefining benign prostatic hyperplasia (BPH) treatment through innovative solutions. Led by practicing urologist Adam Kadlec, the company creates clinically grounded medical devices aimed at improving patient care. Their flagship product, FloStent, is a minimally invasive device designed to restore urinary flow and preserve treatment options, currently in development and clinical trials.

Industries

health-care
hospital-650c
medical-device

Nr. of Employees

small (1-50)


Patents

Intraluminal stent with handle for treating benign prostatic hyperplasia

US-12357479-B2

View Details

Products

Minimally invasive nitinol urethral implant system

A small implantable nitinol device and compatible delivery system designed to be placed via cystoscopy to relieve symptoms of benign prostatic hyperplasia while preserving future treatment options.


Services

Enrollment of qualified patients into investigational device studies with study-related care provided and compensation for time and travel associated with scheduled study visits.

Training and certification of urologists to perform the implant procedure, including proctoring of procedures within clinical studies or early commercial use.

Expertise Areas

  • Benign prostatic hyperplasia (BPH) device therapy
  • Clinical trial management for implantable urology devices
  • Office-based urological procedure workflows
  • Medical device design and engineering
  • Show More (2)

Key Technologies

  • Nitinol-based implantable devices
  • Cystoscopic delivery systems
  • Minimally invasive urological implant procedures
  • Randomized multicenter clinical trial methodologies
  • Show More (1)

News & Updates

Rivermark Medical announced the enrollment of the first patient in its RAPID III clinical study, a trial to evaluate the safety and effectiveness of the FloStent™ System in men with BPH.

The company closed a Series C financing to fund further development of the FloStent system, aiming to provide immediate relief for BPH patients.

The company completed its RAPID-UR study evaluating FloStent in patients with urinary retention due to BPH.

First-in-human procedures performed on 15 patients to evaluate delivery, safety, and effectiveness of FloStent.

Full enrollment of the RAPID-II trial across sites in Australia, New Zealand, and Mexico.


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