FDA.reportPublic FDA data

FEHLING INSTRUMENTS GmbH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
96150053001286223FEHLING INSTRUMENTS GmbH1N2026-01-01Seligenstaedter Str. 100 KARLSTEIN Bavaria DE 63791

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
130191561411676K881412MYOCARD BIOPSY FORCEPDWZ1988-09-08
130191536815354K220981SUPERPLAST Double-Occluder, SUPERPLAST Vascular ProbeDWP2023-04-20
130191820203267K170726Biopsy ForcepsDWZ2017-06-02
130191753924638K153243Fehling-PunchesHAE2016-08-04
130191348664306
130191390601561
130191675215295
130191815030942
130191896712396
130192038464882
130191006246716
130191044304305
130191062015789
130191099700182
130191362180348
130191366900954
130191381258190
130191388615685
130191604082168
130191768965296
130191777512255
130191806966772
130191822011295
130191845595127
130191882767225
130191921456438
130191963601545

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DWZ22017-06-02
DWP12023-04-20
HAE12016-08-04