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Guenter Bissinger Medizintechnik GmbH

FDA Regulatory Profile

Guenter Bissinger Medizintechnik GmbH has 0 FDA recalls, 0 inspections, 6 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 17, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances6Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K213042Supra Non-Stick Bipolar ForcepsNov 17, 2022
K150024Bissinger Monopolar CablesFeb 20, 2015
K051429CLARIS NON-STICK BIPOLAR FORCEPSJul 29, 2005
K042077BITECH BIPOLAR SCISSORSOct 27, 2004
K981919BISSINGER CABLES, CAT. NO. 801000XXAug 6, 1998
K970968BISSINGER DETACHABLE BIPOLAR COAGULATION-FORCEPSMay 21, 1998

FDA data resources