Karex Industries Sdn. Bhd.

FDA Regulatory Profile

Karex Industries Sdn. Bhd. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 11, 2023

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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) clearances8Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K223519Carex Hybrid Personal LubricantAug 11, 2023
K150743Water Based Personal Lubricant with FlavoursNov 12, 2015
K141059NATURAL RUBBER LATEX MALE CONDOMSAug 1, 2014
K132597BLACK COLOURED CONDOMNov 25, 2013
K113056ORANGE COLORED CONDOMS ORANGE SCENTJul 3, 2012
K113061LARGE/EXTRA LAGRE CONDOMDec 7, 2011
K081886KAREX INDUSTRIES MALE NATURAL RUBBER LATEX CONDOM, NON-SPERMICIDAL, LUBRICATED AND NON LUBRICATEDFeb 6, 2009
K070830MALE NATURAL RUBBER LATEX CONDOM (WITH COLORING AND FLAVORING)May 8, 2007