Heather Eisner

FDA Filings

This page includes the latest FDA filings for Heather Eisner. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013744383
FEI Number3013744383
NameHeather Eisner
Owner & OperatorGarrett Leight Europe B.V.
Contact AddressDanzigerbocht 29
Amsterdam NL-NH Noord-Holland 1013AM NL
Official Correspondent
  • Justin Steinhardt
  • 31-20-3330439-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2301 East 7th Street D113
Los Angeles, CA 90023 US
Establishment TypeExport Device to the United States But Perform No Other Operation on Device



FDA Filings

Device
Company
DeviceDate
Heather Eisner [Garrett Leight Europe B.V.]
Mr. Leight2019-05-09
Heather Eisner [Garrett Leight Europe B.V.]
GLCO2019-05-09
Heather Eisner [Garrett Leight Europe B.V.]
Mr. Leight2019-05-09
Heather Eisner [Garrett Leight Europe B.V.]
GLCO2019-05-09

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