Medeon Biodesign Receives FDA 510(k) Clearance for ClickClean(TM) - Laparoscope Lens Cleaning Device

by PRNewswire

LOS ALTOS, Calif. and TAIPEI, Aug. 25, 2015 /PRNewswire/ -- Medeon Biodesign, Inc., a Taiwan medical device company, is pleased to announce that the company has received U.S. Food and Drug Administration 510(k) clearance for ClickClean™, a lens cleaning device. ClickClean provides instant, in-situ, one-click lens cleaning during laparoscopic procedures, which virtually eliminates the need to remove the laparoscope from the body cavity during surgery and significantly reduces the total time, cost, risks and repeated frustration associated with maintaining a clear visual field.

"Impaired vision due to a soiled lens routinely occurs in nearly every surgery.  A soiled lens is one of the disadvantages and most prominent frustrations in performing laparoscopic surgery," said Dr. Thomas Hsu, the original inventor of ClickClean and an urologist at Kaiser Permanente Santa Clara Medical Center, California as well as a Consulting Professor of Urology at Stanford University School of Medicine. "Based on its elegant design to achieve easy and instant lens cleaning, ClickClean could eliminate nearly all of the surgical delays, risks and frustrations associated with existing techniques for laparoscopic lens cleaning."

"ClickClean is a single-use, disposable accessory for laparoscopic surgery, which uses a transparent film to shield the lens from blood, fat, smoke and debris during the surgery by simply clicking a trigger on the device and immediately replacing the soiled film with a segment of new and clean film. It is estimated that 2.8 million laparoscopic procedures are performed in the US and approximately 7.5 million procedures are performed worldwide each year. ClickClean addresses the unmet need of virtually every laparoscopic surgery,"says Dr. Yue-Teh Jang, CEO of Medeon Biodesign.

See the full article here.

With more than 61,000 510(k) summaries to search, including more than 76,000 splash pages (nearly 138,000 records total), quickly find your primary predicate, multiple predicates or reference devices with kBLASTER. Save time with kBLASTER's effective result management features of sorting, My Favorites, Saved Search and Search History from a web browser, so mobile devices or computers can be used interchangeably to build a successful 510(k) clearance strategy. Save money in your 510(k) regulatory strategy and follow-on 510(k) submission spending by enabling self-service extraction of actionable insight from FDA medical device 510(k) clearance summaries.