FDA applicant
Intercure, Ltd.
FDA records 2 decisions for Intercure, Ltd. (Washington, DC) from 2000 to 2002: 2 510(k) clearances. All are in product code HCC (Device, Biofeedback). Its devices cite 1 predicate, 1 of them its own earlier devices. 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 Intercure, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Intercure, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Intercure, 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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