FDA applicant
Thayer Medical Corp.
FDA records 19 decisions for Thayer Medical Corp. (Tucson, AZ) from 1988 to 2024: 19 510(k) clearances. Most are in product codes CAF (Nebulizer (Direct Patient Interface)) and BYH (Drain, Tee (Water Trap)). Its devices cite 4 predicates, 4 of them its own earlier devices. 2 recalls are linked to its devices.
FDA’s records also spell it “Thayer Medical Corporation”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Thayer Medical Corp.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
1in 2016
Class I Class II/III not classified
Planning a device like Thayer 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) Report