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Karl Storz Endoskop GmbH

FDA Regulatory Profile

Karl Storz Endoskop GmbH has 0 FDA recalls, 0 inspections, 11 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 7, 1997

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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) clearances11Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K973068KSEA INSTRUMENT SET FOR SAPHENOUS VEIN HARVESTINGNov 7, 1997
K961702KSEA VAPORIZATION ELECTRODESAug 29, 1996
K953368LUER, JACKSON TRACHEA TUBES, LUER SPEAKING TRACHEA TUBESSep 18, 1995
K943713TORCARS,CANNULAE,SHEATHS,OBTURATORSJun 30, 1995
K951995KARL STORZ CATHETERS, MANDRIN, PLUGS, CONNECTORMay 24, 1995
K943053KSEA SEMM TISSUR PUNCHMar 21, 1995
K943435CHOLANGIOGRAPHY SETNov 7, 1994
K944823KARL STORZ INSULATED DISSECTING CANNULAE, CANNULAE, SUCTION TUBES, INSERT TUBESNov 2, 1994
K943904RIGID TELESCOPESOct 14, 1994
K943697TROCARS,CANNULAE,SHEATHS,OBTURATORSSep 14, 1994
K943816TROCARS,CANNULAE, SHEATHSAug 24, 1994

FDA data resources