FDA.reportPublic FDA data

ALMIKRO GMBH & CO. KG

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30091348553009134855ALMIKRO GMBH & CO. KG1N2026-01-01Loewenweg 1e Bad Krozingen Baden-Wurttemberg DE 79189

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2188561207203739K982658KSEA ENDOSCOPES FOR DENTAL PROCEDURESEIA1998-10-15
2188561369306560K945787KARL STORZ SEMI-RIGID MICRO-ENDOSCOPES AND ACCESSORIES FOR ENDOSCOPIC ARTHROSCOPY PROCEDURESHRX1995-06-13
2188561236691219K940464KARL STORZ URETERO-RENOSCOPE/URETERSCOPEFGB1994-06-24
2188561618295929K170462KARL STORZ ShuntScopeGWG2017-05-16
2188561034572600
2188561395629435
2188561422140012
2188561629076280
2188561733380877
2188561742094899
2188561754777346
2188561775127890

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GWG12017-05-16
EIA11998-10-15
HRX11995-06-13
FGB11994-06-24