Guenter Bissinger Medizintechnik GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
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) cleared devices by Guenter Bissinger Medizintechnik GmbH
6 devices
Cleared
Nov 17, 2022
Supra Non-Stick Bipolar Forceps
General & Plastic Surgery
421d
Cleared
Feb 20, 2015
Bissinger Monopolar Cables
General & Plastic Surgery
44d
Cleared
Jul 29, 2005
CLARIS NON-STICK BIPOLAR FORCEPS
General & Plastic Surgery
58d
Cleared
Oct 27, 2004
BITECH BIPOLAR SCISSORS
General & Plastic Surgery
86d
Cleared
Aug 06, 1998
BISSINGER CABLES, CAT. NO. 801000XX
General & Plastic Surgery
66d
Cleared
May 21, 1998
BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPS
Obstetrics & Gynecology
430d