Guenter Bissinger Medizintechnik GmbH

Guenter Bissinger Medizintechnik GmbH holds 6 FDA 510(k) medical device clearances, first cleared 1998, most recent 2022.

Top product codes for Guenter Bissinger Medizintechnik GmbH

GEI — General, Plastic Surgery5 devices
HET — Obstetrics/Gynecology1 device

Recent clearances by Guenter Bissinger Medizintechnik GmbH

K213042 — Supra Non-Stick Bipolar ForcepsCode GEI·2022-11-17
K150024 — Bissinger Monopolar CablesCode GEI·2015-02-20
K051429 — CLARIS NON-STICK BIPOLAR FORCEPSCode GEI·2005-07-29
K042077 — BITECH BIPOLAR SCISSORSCode GEI·2004-10-27
K981919 — BISSINGER CABLES, CAT. NO. 801000XXCode GEI·1998-08-06
K970968 — BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPSCode HET·1998-05-21

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