Boehringer Laboratories - FDA 510(k) Cleared Devices

Boehringer Laboratories is a family-owned American medical technology company headquartered in Phoenixville, Pennsylvania, with operations in McHenry, US. The company specializes in respiratory therapy and minimally invasive surgical devices.

Boehringer Laboratories has maintained a strong FDA 510(k) regulatory record since 1976. The company has received 38 FDA 510(k) clearances from 38 total submissions, with no denied submissions. Recent clearances span 2024, demonstrating continued active development. The company's portfolio focuses primarily on anesthesiology devices, including autotransfusion and wound management systems, alongside general hospital and surgical suction equipment.

Notable product lines include the AUTOVAC series for closed wound autotransfusion and the ViSiGi 3D Gastric Sizing Tube for gastroenterology applications. The company's innovations have earned US and foreign patents in respiratory therapy and minimally invasive surgery technologies.

Explore the complete list of device names, product codes, and clearance dates in the database to review Boehringer Laboratories' full regulatory history and current cleared devices.