FDA applicant
Maxol Limited L.C.
FDA records 1 decision for Maxol Limited L.C. (Overland Park, KS) in 1995: 1 510(k) clearance. All are in product code KCZ (Prosthesis, Breast, External, Used With Adhesive). 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 Maxol Limited L.C.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Maxol Limited L.C. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Maxol Limited L.C.’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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