Genci Omari

FDA Filings

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

FDA Registration(s)
Registration Number3012037425
FEI Number3012037425
NameGenci Omari
Owner & OperatorVITREQ BV
Contact AddressSeggelant-Noord 2
Vierpolders NL-ZH Zuid-Holland 3237 MG NL
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address500 TOTTEN POND RD STE 10
WALTHAM, MA 02451 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Genci Omari [VITREQ BV]
VitreQ Directional Laser Probe2019-05-03
Genci Omari [VITREQ BV]
VitreQ Chandelier & Light Fibers2019-05-03
Genci Omari [VITREQ BV]
VitreQ Directional Laser Probe2019-05-03
Genci Omari [VITREQ BV]
VitreQ Chandelier & Light Fibers2019-05-03
Genci Omari [VITREQ BV]
VitreQ Directional Laser Probe2019-05-03
Genci Omari [VITREQ BV]
VitreQ Chandelier & Light Fibers2019-05-03
Genci Omari [VITREQ BV]
VitreQ Light Source Adaptor2019-05-03
Genci Omari [VITREQ BV]
Depressor, orbital2016-09-06
Genci Omari [VITREQ BV]
Spatula, Ophthalmic2016-09-06
Genci Omari [VITREQ BV]
FORCEPS, OPHTHALMIC2015-11-18
Genci Omari [VITREQ BV]
VITREQ Scissors2015-11-18
Genci Omari [VITREQ BV]
VITREQ Cannula2015-11-18
Genci Omari [VITREQ BV]
VITREQ Needle2015-11-18

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