FDA applicant
Divi Intl. Co.
FDA records 1 decision for Divi Intl. Co. (Miami, FL) in 1999: 1 510(k) clearance. All are in product code IMC (Bath, Paraffin). 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 Divi Intl. Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Divi Intl. Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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