Gunter Bissinger Medizintechnik GmbH

FDA Regulatory Profile

Gunter Bissinger Medizintechnik GmbH has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 5, 2018

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K172368Bipolar Micro-Coagulation ForcepsApr 5, 2018
K033177POWERGRIP BIPOLAR COAGULATION FORCEPS, MODEL 824XXXXXMar 11, 2004