FDA applicant
Klarity Medical & Equipment (GZ) Co., Ltd.
FDA records 3 decisions for Klarity Medical & Equipment (GZ) Co., Ltd. (Guangzhou, CN) from 2021 to 2025: 3 510(k) clearances. All are in product code IYE (Accelerator, Linear, Medical). Since 2016 its 510(k)s took a median of 249 days from receipt to decision, against 170 for FDA’s reviews in the same codes and years. Its devices cite 2 predicates, 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 Klarity Medical & Equipment (GZ) Co., 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 2021.
Planning a device like Klarity Medical & Equipment (GZ) Co.…’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) ReportOther applicant names beginning “Klarity”
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