FDA.reportPublic FDA data

STORZ MEDICAL AMERICA, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
10611581000511585STORZ MEDICAL AMERICA, INC.1Y2026-01-011000 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
3139751671646900P920051STORZ MODULITH (TM) LITHOTRIPTERLNS1995-02-17
3139751761178919P080028STORZ MEDICAL DUOLITH SD1 SHOCK WAVE THERAPYNBN2016-01-08
3139751594610251K203710Storz Medical MAGNETOLITH Muscle StimulatorIPF2021-05-03
3139751400958909K202112Storz Medical Duolith SD1 T-Top & Tower System with C-Actor Sepia HandpiecePZL2021-02-21
3139751174458313K201001Modulith SLX-F2LNS2021-03-30
3139751720602827K200965XR-MX/1000JAA2020-12-29
3139751007557140K173692D-Actor 200 Vibration Massage SystemISA2018-04-13
3139751295719024K120769MODULTH SLKLNS2012-06-12
3139751417013560K093603STORM-BASE 2.0LLZ2010-03-18
3139751587620619K072788STORZ MODULITH LITHOTRIPTER SLX-F2-F180LNS2007-12-26
3139751270717785K070579STORZ SLX-F2 STORM TOUCHLNS2007-08-30
3139751571044689K040476STORZ MODULITH, MODEL SLX-F2LNS2004-08-26
3139752051427730K012482STORZ MODULITH SLK LITHOTRIPTER WITH MULTIVIEW OPTIONLNS2001-10-16
3139751152879716K011700MODULITH SLK LITHOTRIPTERLNS2002-08-16
3139751196244068K010340MODULITH LITHOTRIPSY, MODEL SLK FOR THE FRAGMENTATION OF URINARY AND UPPER URETERAL CALCULILNS2001-02-13
3139751329028153K004037X-RAY SYSTEM XR-MXJAA2001-02-02
3139751838369637

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LNS82021-03-30
JAA22020-12-29
IPF12021-05-03
PZL12021-02-21
ISA12018-04-13
NBN12016-01-08
LLZ12010-03-18
LNS 11995-02-17