FDA applicant
Geon Corporation
FDA records 5 decisions for Geon Corporation (Syosset, NY) from 1996 to 2025: 5 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and BTA (Pump, Portable, Aspiration (Manual Or Powered)). Its devices cite 1 predicate, 1 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Geon Corp.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Geon Corporation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Geon Corporation’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