Gunter Bissinger Medizintechnik GmbH

Gunter Bissinger Medizintechnik GmbH holds 2 FDA 510(k) medical device clearances, first cleared 2004, most recent 2018.

Top product codes for Gunter Bissinger Medizintechnik GmbH

GEI — General, Plastic Surgery1 device
HET — Obstetrics/Gynecology1 device

Recent clearances by Gunter Bissinger Medizintechnik GmbH

K172368 — Bipolar Micro-Coagulation ForcepsCode GEI·2018-04-05
K033177 — POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXXCode HET·2004-03-11

Data sourced from openFDA. This site is unofficial and independent of the FDA.