FDA.reportPublic FDA data

ENDOPLUS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
14237143000719482ENDOPLUS1N2026-01-01750 Tower Rd Ste A Mundelein IL US 60060

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
744481173742438K925114LAPAROSCOPIC INSTRUMENTSHFI1994-02-28
744481010339775K925079LAPAROSCOPIC INST. (SCISSORS,FORCEPS,NEEDLEHOLDER)HET1994-08-24
744481064929965K151567ENDOPLUS hand-held laparoscopic instrumentsHFI2015-12-23
744481481760166
744481977574753

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
HFI22015-12-23
HET11994-08-24

PMN#

GUDID#

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