FDA applicant
Careverse Technology Pte., Ltd.
FDA records 1 decision for Careverse Technology Pte., Ltd. (Singapore, SG) in 2025: 1 510(k) clearance. All are in product code QIH (Automated Radiological Image Processing Software). 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 Careverse Technology Pte., Ltd.’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 2025.
Planning a device like Careverse Technology Pte., 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