FDA applicant
Wellspring Pharmaceutical Corporation
FDA records 1 decision for Wellspring Pharmaceutical Corporation (Sarasota, FL) in 2021: 1 510(k) clearance. All are in product code MVV (Device, Acupressure). Its devices cite 2 predicates, 0 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 Wellspring Pharmaceutical Corporation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2021
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
Planning a device like Wellspring Pharmaceutical Corporation’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