FDA applicant
Leemart Bedding Mfg. Co.
FDA records 1 decision for Leemart Bedding Mfg. Co. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code IKY (Mattress, Flotation Therapy, Non-Powered). 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 Leemart Bedding Mfg. Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Leemart Bedding Mfg. Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Leemart Bedding Mfg. Co.’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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