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Medipurpose Pte. , Ltd.

FDA Regulatory Profile

Medipurpose Pte. , Ltd. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Sep 22, 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) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K222224SurgiLance® Safety LancetSep 22, 2022
K130132BABYLANCE HEEL INCISION DEVICEFeb 11, 2013
K110062MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AGSep 1, 2011
K101145SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250Oct 21, 2010
K101417BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200Oct 19, 2010

FDA data resources