FDA.reportPublic FDA data

KARL STORZ LITHOTRIPSY-AMERICA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
10611581000511585KARL STORZ LITHOTRIPSY-AMERICA, INC.1Y2020-04-251000 COBB PLACE BLVD BUILDING 400, SUITE 450 Kennesaw GA US 30144

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
156012014395376P920051STORZ MODULITH (TM) LITHOTRIPTERLNS1995-02-17
156011885087776P080028STORZ MEDICAL DUOLITH SD1 SHOCK WAVE THERAPYNBN2016-01-08
156011539718399K120769MODULTH SLKLNS2012-06-12
156011100007570K093603STORM-BASE 2.0LLZ2010-03-18
156011787334732K072788STORZ MODULITH LITHOTRIPTER SLX-F2-F180LNS2007-12-26
156011417989439K070579STORZ SLX-F2 STORM TOUCHLNS2007-08-30
156011514420212K040476STORZ MODULITH, MODEL SLX-F2LNS2004-08-26
156011512692645K004037X-RAY SYSTEM XR-MXJAA2001-02-02

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LNS42012-06-12
NBN12016-01-08
LLZ12010-03-18
JAA12001-02-02
LNS 11995-02-17

PMN#