FDA applicant
Veran Medical Technologies, Inc.
FDA records 7 decisions for Veran Medical Technologies, Inc. (St. Louis, MO) from 2006 to 2021: 7 510(k) clearances. Most are in product codes JAK (System, X-Ray, Tomography, Computed) and EOQ (Bronchoscope (Flexible Or Rigid)). Its devices cite 11 predicates, 6 of them its own earlier devices. 15 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Veran Medical Technologies, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2021
2026 so far, outlined.
Recalls per year
14in 2023
Class I Class II/III not classified
Planning a device like Veran Medical Technologies, Inc.’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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