Abraham Farhan

FDA Filings

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

FDA Registration(s)
Registration Number8040449
FEI Number3002501070
NameAbraham Farhan
Owner & OperatorOPHTEC BV
Contact AddressSchweitzerlaan 15
Groningen NL-GR Groningen 9728 NL
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressSawgrass Executive Center 400 Sawgrass Corporate Pkwy, Suite 220
Sunrise, FL 33325 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Abraham Farhan [OPHTEC BV]
StabilEyes Capsular Tension Ring2007-12-05
Abraham Farhan [OPHTEC BV]
RingJect2007-12-05
Abraham Farhan [OPHTEC BV]
Ophtec Capsular Tension Ring2007-12-05
Abraham Farhan [OPHTEC BV]
Verisyse - Veriflex Enclavation Needle2007-12-05
Abraham Farhan [OPHTEC BV]
Artisan - Artiflex Enclavation Needle2007-12-05
Abraham Farhan [OPHTEC BV]
StablEyes Capsular Tension Ring Inserter2007-12-05
Abraham Farhan [OPHTEC BV]
Easy Control Micro Inserter2007-12-05
Abraham Farhan [OPHTEC BV]
Verisyse Myopia Phakic Lens2004-12-15
Abraham Farhan [OPHTEC BV]
Veriflex Myopia Phakic Lens2004-12-15
Abraham Farhan [OPHTEC BV]
Artisan Myopia Phakic Lens2004-12-15
Abraham Farhan [OPHTEC BV]
Artiflex Myopia Phakic Lens2004-12-15

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