Cardica, a medical device company, has received 510(k) approval from the US Food and Drug Administration (FDA) for its MicroCutter Xchange 30 device and blue staple cartridge for medium thickness tissue. The company has designed the ...
Tags: Cardica, medical device
Ethicon Endo-Surgery has obtained 510(k) approval from the US Food and Drug Administration (FDA) for its HARMONIC FOCUS+ shears with adaptive tissue technology. HARMONIC FOCUS+ now brings adaptive tissue technology to open procedures ...
Tags: Ethicon, HARMONIC FOCUS+, adaptive tissue, technology, HARMONIC
Ethicon Endo-Surgery, a subsidiary of Johnson & Johnson, has obtained 510(k) approval from the US Food and Drug Administration (FDA) for an expanded indication of ear, nose and throat (ENT) procedures for the ENSEAL tissue sealers. The ...
Century Medical, a Japanese medical device distributor, has sought clearance from the country's Pharmaceuticals and Medical Devices Agency (PMDA) for Cardica's MicroCutter XCHANGE 30 cutting and stapling cartridge, which is intended for ...
Olympus has gained 510(k) clearance from the US Food and Drug Administration (FDA) for its Articulating HD 3D laparoscopic surgical video system. The system, ENDOEYE FLEX 3D, when compared with conventional 2D surgical systems reduces ...
Tags: Olympus, FDA Nod, Flex 3D System
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Teleflex Incorporated's new line of Weck reusable obturators, designed for use during laparoscopic procedures. The stainless steel obturators, which are ...
Tags: FDA, laparoscopic procedure, medical tool, medical technology
Teleflex has launched complete line of Weck Access devices including Weck Vista bladeless access ports and Weck EFx Endo Fascial Closure system, designed for use during laparoscopic procedures. The company said during minimally invasive ...
Tags: Teleflex, Weck Access devices, laparoscopic procedures