FDA applicant
Silq Technologies Corporation
FDA records 3 decisions for Silq Technologies Corporation (Sunny Isles Beach, FL) from 2022 to 2024: 3 510(k) clearances. All are in product code EZL (Catheter, Retention Type, Balloon). Its devices cite 3 predicates, 2 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Silq Technologies, Corp.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Silq Technologies Corporation’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2022.
Planning a device like Silq Technologies 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