ClearanceBrief
510(k) K212510 ยท FTC Light, Ultraviolet, Dermatological

7 Series Phototherapy Device

ApplicantDaavlin Distributing Co., Bryan OH, US
DecisionSubstantially Equivalent, Nov 4, 2021
ReceivedAug 10, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K212510

DateFirm and productCodeLinked 510(k)
Jul 15, 2026Daavlin Distributing Company
Photera 600, phototherapy device; Ultraviolet Lamp For Dermatologic Disorders
Open, Classified
FTCNone listed

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