FDA applicant
Corvent Medical, Inc.
FDA records 2 decisions for Corvent Medical, Inc. (Fargo, ND) from 2024 to 2026: 2 510(k) clearances. Most are in product codes CBK (Ventilator, Continuous, Facility Use) and MOD (Accessory To Continuous Ventilator (Respirator)). Its devices cite 2 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “CorVent® Medical, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Corvent Medical, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Corvent Medical, 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