ClearanceBrief
510(k) K262300 ยท EBI Resin, Denture, Relining, Repairing, Rebasing

Denture Base Resin V2

ApplicantFormlabs Ohio, Inc., Millbury OH, US
DecisionSubstantially Equivalent, Jul 8, 2026
ReceivedJul 7, 2026
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K262300

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.