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Compactcath, Inc.

FDA Regulatory Profile

Compactcath, Inc. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jun 14, 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) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K180738COMPACTCATH Lubricated Intermittent UrinaryCatheter and OneCath Intermittent Urinary CatheterJun 14, 2018
K160858CompactCath Intermittent Urinary CatheterApr 26, 2016
K140945COMPACTCATH INTERMITTENT URINARY CATHETERAug 22, 2014

FDA data resources