FDA applicant
Chi'Am Intl.
FDA records 1 decision for Chi'Am Intl. (Circle Pines, MN) in 1993: 1 510(k) clearance. All are in product code LRL (Cushion, Hemorrhoid). 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 Chi'Am Intl.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Chi'Am Intl. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Chi'Am Intl.’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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