FDA applicant
Manexim Multicorp, Ltd.
FDA records 5 decisions for Manexim Multicorp, Ltd. (Canada Law1v6, CA) from 1985 to 1986: 5 510(k) clearances. All are in product code HIS (Condom). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Manexim Multicorp, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Manexim Multicorp, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Manexim Multicorp, Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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