FDA applicant
Shenzhen Amydi-Med Electrics Tech Co., Ltd.
FDA records 1 decision for Shenzhen Amydi-Med Electrics Tech Co., Ltd. (Shenzhen, CN) in 2024: 1 510(k) clearance. All are in product code GXY (Electrode, Cutaneous). 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 Shenzhen Amydi-Med Electrics Tech Co., Ltd.’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.
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