FDA applicant
Convertors
FDA records 10 decisions for Convertors (Mchenry, IL) from 1977 to 1979: 10 510(k) clearances. Most are in product codes KKX (Drape, Surgical, Antimicrobial) and EFQ (Gauze/Sponge, Internal). 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 Convertors’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Convertors since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Convertors’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