FDA applicant
Arineta, Ltd.
FDA records 5 decisions for Arineta, Ltd. (Caesarea, IL) from 2016 to 2025: 5 510(k) clearances. All are in product code JAK (System, X-Ray, Tomography, Computed). Since 2016 its 510(k)s took a median of 245 days from receipt to decision, against 139 for FDA’s reviews in the same codes and years. Its devices cite 6 predicates, 4 of them its own earlier devices. 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 Arineta, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2016.
Planning a device like Arineta, 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