Olympus Receives Fda Clearance for Powerseal™ Open Extended Jaw Device

Olympus Receives FDA Clearance for Open Surgery Sealing Device

The new Powerseal Open Extended Jaw device is the fourth addition to the company’s advanced bipolar surgical energy portfolio. Olympus Corp announced it has received 510(k) clearance from the US Food and Drug Administration for its Powerseal Open Extended Jaw Sealer/Divider, a device intended for use in open surgery. The device is the latest addition to the Olympus Powerseal portfolio of advanced bipolar surgical energy products, joining three e…

Olympus gains FDA clearance for POWERSEAL Open Extended Jaw Device

Olympus Corporation has received FDA 510(k) clearance for the POWERSEAL Open Extended Jaw Sealer/Divider. This latest edition to the Olympus POWERSEAL advanced bipolar surgical energy portfolio supports clinical needs for precision, efficiency and control during surgery.The POWERSEAL Open Extended Jaw Sealer/Divider joins three 5mm devices in the POWERSEAL portfolio. These 5mm devices are offered in three jaw configurations, each available in th…