ClearanceBrief
510(k) K262285 ยท FTC Light, Ultraviolet, Dermatological

UV Phototherapy Device (KZX-308nm-BL65, KZX-308nm-BL55, KZX-308nm-BL50, KZX-308nm-BL45, KZX-308nm-BL35)

ApplicantShijiazhuang Recovery Star Medical Device Co., Ltd., Shijiazhuang, CN
DecisionSubstantially Equivalent, Oct 5, 2026
ReceivedJul 6, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K262285

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.