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Microspecialties LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
12260743002616700Microspecialties LLC1N2026-01-01430 Smith St Middletown CT US 06457

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2033421275577574K994015ACCUBLADE (ACS MODEL), MK8507, ACCUBLADE (HANSOTOME MODEL), MK8508HNO2000-03-15
2033421966428833K980510KERATOME BLADE (135 MICRON, MODEL 300135), (160 MICRON, MODEL 300160), (200 MICRON, MODEL 30020)HNO1998-05-01
2033421867894077K093753MDPO FRAME SYSTEMKTT2010-08-26
2033421740801367K050851DELTA PUNCTUM PLUGLZU2005-08-19
2033421056160274K033457M2 COMPATIBLE MICROKERATOME BLADEHNO2004-05-25
2033421723294675K020482KERATOME BLADE 200200 & 600600HNO2002-12-16
2033421295583796K011195PRIZM BLADE (MORIA MODEL) LSK / MK8510LSK; PRIZM BLADE (MORIA MODEL) CB / MK8511CBHNO2001-11-06
2033421044550507
2033421057948084
2033421166404499
2033421436067451
2033421667959035
2033421676064140
2033421699339434
2033421443446787
2033421900391316
2033422069842675

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HNO102004-05-25
LZU22005-08-19
KTT12010-08-26

PMN#