Garrett Leight Europe B V

FDA Filings

This page includes the latest FDA filings for Garrett Leight Europe B V. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)

• Registration Number: 3013744383
• FEI Number: 3013744383
• Name: Heather Eisner
• Owner & Operator: Garrett Leight Europe B.V.
• Contact Address: Danzigerbocht 29 ; Amsterdam NL-NH Noord-Holland 1013AM NL
• Official Correspondent:
  • Justin Steinhardt
  • 31-20-3330439-x
• US Agent:
  • Heather Eisner
  • Garrett Leight, LLC
  • 310 3922100
  • heather@garrettleight.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 2301 East 7th Street D113; Los Angeles, CA 90023 US
• Establishment Type: Export Device to the United States But Perform No Other Operation on Device

FDA Filings

Device Company	Device	Date
HQZ Heather Eisner [Garrett Leight Europe B.V.]	Mr. Leight	2019-05-09
HQZ Heather Eisner [Garrett Leight Europe B.V.]	GLCO	2019-05-09
HQY Heather Eisner [Garrett Leight Europe B.V.]	Mr. Leight	2019-05-09
HQY Heather Eisner [Garrett Leight Europe B.V.]	GLCO	2019-05-09

U.S. Import Records [external site]

Import ID	Shipment	Cargo Description	Quantity
2018100133193	Anvers,Belgium -> Los Angeles, California	EYE WEAR CASE	140 PKG