Profile: Uromedica, Inc. develops minimally invasive medical devices. We offer products for urinary incontinence and related disorders. We provide products under the ACT® and ProACT™ brands, based on patented adjustable balloon technology. We offer adjustable continence therapy investigation devices for both the female and male patient population.
The company was founded in 1997, has revenues of < USD 1 Million and is ISO 9001, CE certified.
FDA Registration Number: 3003477176
4 Products/Services (Click for related suppliers)
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• Manual Gastro-Urology Surgical Instrument (FDA Code: KOA / 876.4730) A manual gastroenterology-urology surgical instrument and accessories is a device designed to be used for gastroenterological and urological surgical procedures. The device may be nonpowered, hand-held, or hand-manipulated. Manual gastroenterology-urology surgical instruments include the biopsy forceps cover, biopsy tray without biopsy instruments, line clamp, nonpowered rectal probe, nonelectrical clamp, colostomy spur-crushers, locking device for intestinal clamp, needle holder, gastro-urology hook, gastro-urology probe and director, nonself-retaining retractor, laparotomy rings, nonelectrical snare, rectal specula, bladder neck spreader, self-retaining retractor, and scoop. |
• Mechanical/Hydraulic Incontinence Device (FDA Code: EZY / 876.5280) An implanted mechanical/hydraulic urinary continence device is a device used to treat urinary incontinence by the application of continuous or intermittent pressure to occlude the urethra. The totally implanted device may consist of a static pressure pad, or a system with a container of radiopaque fluid in the abdomen and a manual pump and valve under the skin surface that is connected by tubing to an adjustable pressure pad or to a cuff around the urethra. The fluid is pumped as needed from the container to inflate the pad or cuff to pass on the urethra. |
• Minimally Invasive Medical Devices |
• Urinary Incontinence Disorder Systems |