FDA applicant
Verimed Holdings, Inc.
FDA records 12 decisions for Verimed Holdings, Inc. (Fort Lauderdale, FL) from 1983 to 1998: 12 510(k) clearances. Most are in product codes HCC (Device, Biofeedback) and HIR (Perineometer). Its devices cite 2 predicates, 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 Verimed Holdings, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Verimed Holdings, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Verimed Holdings, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report