FDA applicant
Everest Medical Corp.
FDA records 21 decisions for Everest Medical Corp. (Minneapolis, MN) from 1987 to 2000: 21 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and KNS (Unit, Electrosurgical, Endoscopic (With Or…). Its devices cite 6 predicates, 6 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 Everest Medical Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Everest Medical Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Everest Medical Corp.’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) ReportOther applicant names beginning “Everest”
FDA records each applicant name separately; these may or may not be the same firm.