Apyx medical corporation announces fda 510(k) clearance for the renuvion® micro handpiece

Clearwater, fla.--(business wire)--apyx medical corporation (nasdaq:apyx) (the “company”), the manufacturer of a proprietary helium plasma and radiofrequency technology marketed and sold as renuvion®, today announced it has received 510(k) clearance from the u.s. food and drug administration (“fda”) for the renuvion micro handpiece, a new addition to the renuvion product family. the renuvion micro handpiece is cleared with an indication “for the delivery of radiofrequency energy and/or helium p.
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