Lombart Instrument Inc D B A Marco Ophthalmic

FDA Filings

This page includes the latest FDA filings for Lombart Instrument Inc D B A Marco Ophthalmic. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1041845
FEI Number1041845
NameLombart Instrument, Inc. d/b/a Marco Ophthalmic
Owner & OperatorLombart Instrument, Inc. d/b/a Marco Ophthalmic
Contact Address11825 CENTRAL PKWY. --
Jacksonville FL 32224 US
Official Correspondent
  • Cheryl Bennett
  • x-904-6429330-132
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address11825 CENTRAL PKWY.
Jacksonville, FL 32224 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Lombart Instrument, Inc. d/b/a Marco Ophthalmic
Brightness Acuity Tester2008-03-12

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