ClearanceBrief
510(k) K262885 ยท FTC Light, Ultraviolet, Dermatological

308nm Ultraviolet Light Therapy Device (XWYL-401A, XWYL-403A)

ApplicantGuangxi Hope Medical Devices Technology Co., Ltd., Yulin, CN
DecisionSubstantially Equivalent, Oct 14, 2026
ReceivedAug 17, 2026
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K262885

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.