FDA applicant
Etview, Ltd.
FDA records 9 decisions for Etview, Ltd. (Binyamina, IL) from 2005 to 2018: 9 510(k) clearances. Most are in product codes BTR (Tube, Tracheal (W/Wo Connector)) and CBI (Tube, Tracheal/Bronchial, Differential…). Its devices cite 16 predicates, 7 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Etview”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Etview, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2018
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Etview, Ltd.’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