FDA.reportPublic FDA data

Allison Orsley

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30089660753008966075Allison Orsley1N2026-01-01581 Inner Cir Lady Lake FL US 32162

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1310711704809712K253248Bright Cavity LinerEJK2026-01-13
1310711112975871K252469MAGNABOND SE; MAGNABOND UNIVERSAL; MAGNABOND UNIVERSAL DCAKLE2025-11-06
1310711604051826K192830Bright Temporary C&BEBG2020-09-02
1310711420694203K121915BRIGHT RESTORATIVE MATERIALSEBF2012-09-28
1310711372008584K102836BONASIL A+ IMPRESSION MATERIALSELW2011-01-13
1310711842050315K102257NANOCERAM- BRIGHTEBF2010-11-19
1310711513916511K102255DMP ETCHING GELEBF2010-11-23
1310711185660577K102254DMP SINGLE BONDINGKLE2010-11-23
1310711566335939K102252DMP PIT & FISSURE SEALANTEBC2010-12-03
1310711105729547
1310711572630262

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EBF32012-09-28
KLE22025-11-06
EJK12026-01-13
EBG12020-09-02
ELW12011-01-13
EBC12010-12-03