Shinva Medical Instrument announced that its subsidiary, Shinva Surgical Instruments, received Class III medical device registration certificates from the National Medical Products Administration on September 22, 2026, covering three products. The approved products include a plasma surgical device, which consists of a main unit, power cord, foot switch, and flow controller. Used together with the company's single-use plasma surgical electrodes, it is intended for cutting, vaporization, and coagulation of ear, nose, and throat soft tissue in endoscopic and open surgeries under a saline environment. The other two products are a single-use electric linear cutting stapler with reloads, and a single-use electric linear cutting stapler and reload assembly, suitable for transection, resection, and anastomosis of the esophagus, stomach, and intestines. The assembly has a similar scope of application and uses RFID radio-frequency identification technology and a universal-fit structural design. Shinva Medical Instrument stated that the registration certificates obtained by its subsidiary will create synergy with the company's existing medical endoscope camera systems and minimally invasive endoscopic surgical instruments, expanding the service boundaries of its overall minimally invasive surgery solutions and strengthening the company's comprehensive competitiveness in the field of minimally invasive surgery.
Shinva Medical Instrument Co LtdSubsidiary received Class III registration certificates for three new surgical devices, expanding its minimally invasive surgery product portfolio.
