Kls Martin GmbH + Co. KG

FDA Regulatory Profile

Kls Martin GmbH + Co. KG has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 11, 2019

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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
K183526Codman Electrosurgical Generator, Foot PedalApr 11, 2019
K081678CONMED BEAMER SYSTEM C600Jul 29, 2008