FDA applicant
Sterex Electrolysis Intl., Ltd.
FDA records 1 decision for Sterex Electrolysis Intl., Ltd. (Birmingham, GB) in 1995: 1 510(k) clearance. All are in product code KCW (Epilator, High Frequency, Needle-Type). 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 Sterex Electrolysis Intl., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Sterex Electrolysis Intl., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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