Medical Device Manufacturer · DE , Muehlheim, Baden-Wuerttemberg

Guenter Bissinger Medizintechnik GmbH - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1998

Total

Cleared

Denied

Guenter Bissinger Medizintechnik GmbH has 6 FDA 510(k) cleared medical devices. Based in Muehlheim, Baden-Wuerttemberg, DE.

Last cleared in 2022. Active since 1998. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Guenter Bissinger Medizintechnik GmbH Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Guenter Bissinger Medizintechnik GmbH

6 devices

1-6 of 6