FDA applicant
Curio Digital Therapeutics, Inc.
FDA records 1 decision for Curio Digital Therapeutics, Inc. (Princeton, NJ) in 2024: 1 510(k) clearance. All are in product code SAP (Computerized Behavioral Therapy Device For…). Its devices cite 1 predicate, 0 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 Curio Digital Therapeutics, Inc.’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 2024.
Planning a device like Curio Digital Therapeutics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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