ClearanceBrief
510(k) K093321 ยท DZE Implant, Endosseous, Root-Form

BIOHORIZONS LASER-LOK 3.0 IMPLANT SYSTEM

ApplicantBioHorizons Implant Systems, Inc., Birmingham AL, US
DecisionSubstantially Equivalent, Apr 2, 2010
ReceivedOct 23, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K093321

DateFirm and productCodeLinked 510(k)
Feb 5, 2025DDS Lab
Temporary Titanium Abutments
Open, Classified
NHANone listed

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