FDA applicant
Wenzhou Lingfeng Electronic Technology Co., Ltd.
FDA records 2 decisions for Wenzhou Lingfeng Electronic Technology Co., Ltd. (Ruian, CN) from 2021 to 2026: 2 510(k) clearances. All are in product code IRP (Massager, Powered Inflatable Tube). 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 Wenzhou Lingfeng Electronic Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2021
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2021.
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