The path to 510(k) submission defined after FDA feedback
Based on the feedback from the FDA, Biovica has now a clear path to a 510(k) submission and…
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28 Aug 19
Based on the feedback from the FDA, Biovica has now a clear path to a 510(k) submission and…
27 Aug 19
Biobeat's products enable cloud-based healthcare with connectivity either through a smartphone or a dedicated gateway
22 Aug 19
A drug-free treatment for blood-borne diseases that uses a magnetic sieve to remove infected blood cells from a…
21 Aug 19
The Q-Sera technology is based on lead active RAPClot which has been shown to rapidly produce high-quality serum…
21 Aug 19
DiLumen Ik knife is part of a growing platform of accessories that work in conjunction with the second-generation…
20 Aug 19
Idiopathic scoliosis is the most common spinal deformity in children and is most often diagnosed between ages 10…
20 Aug 19
The FDA approval allows patients to undergo a full-body MRI1 while benefiting from the latest advances in DBS
19 Aug 19
FDA has approved the Sapien 3 and Sapien 3 Ultra for Edwards Lifesciences, and the CoreValve Evolut R…
19 Aug 19
Barostim Neo is one of the first therapies to receive the FDA's breakthrough device designation
16 Aug 19
The ARTAS Robotic Hair Restoration System is the first and only hair restoration system in the world combining…