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Biim Ultrasound receives 510(k) clearance by the FDA

biim ultrasound

Norwegian Biim Ultrasound announced October 27th that their Biim linear probe and Biim software app received FDA clearance as a diagnostic ultrasound system.

The Biim Diagnostic Ultrasound System is intended for diagnostic ultrasound imaging for the human body. Specific clinical applications include musculoskeletal, needle guidance, pediatric, peripheral vessel and small organs.

“This is a great milestone achievement for the company. We can start realizing our vision of making ultrasound accessible for everyone in the medical space. We have broken the code for achieving high performance and low cost. The Biim concept is disruptive; a wireless pocket sized ultrasound product, affordable and easy to use with image display on tablets and phones,” said Rune Nystad, CEO and founder of Biim Ultrasound.

The Biim concept is being launched December 2017.