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News Release - April 15, 2022
SonoScape receives FDA 510(k) clearance for HD-550 Endoscopy system
SHENZHEN, China, April 15, 2022 -- (Healthcare Sales & Marketing Network) -- On April 15th, SonoScape today announced that the U.S. Food and Drug Administration (FDA) has approved its flagship video endoscopy system HD-550 for gastrointestinal diagnosis, setting up a major milestone on SonoScape's Endoscopic product roadmap.The HD-550 endoscopy system has been available outside of the USA since 2019. By 2021, HD550's top-of-the-line features and quality combined with its versatility saw it installed in close to 40 countries around the world and has made SonoScape the third best-selling brand in China.
"We have grown into a trusted name in the global endoscopy industry, we are now ready to extend our offerings to the USA healthcare providers." Steven He, Sales Director of SonoScape Endoscopy commented, "This FDA clearance opens up opportunities in one of the world's biggest endoscopy markets, indeed is a powerful boost of our brand recognition, and a tremendously important phase of business development in SonoScape's 20 years' history".
About SonoScape
Founded in 2002 in Shenzhen China, SonoScape has committed itself to "Caring for Life through Innovation" by providing ultrasound and endoscopy solutions. With seamless support, SonoScape provides worldwide sales and service in more than 130 countries, benefiting local hospitals and doctors with comprehensive imaging diagnostic evidence and technical support. Investing 20% of total revenue into R&D annually, SonoScape establishes seven R&D centers in Shenzhen, Shanghai, Harbin, Wuhan, Tokyo, Seattle, and Silicon Valley, with more advanced products to be introduced into the pipeline.
For more information, please visit us at https://sonoscape.com/.
Source: SonoScape Medical
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