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 Number: 8040449
• FEI Number: 3002501070
• Name: Abraham Farhan
• Owner & Operator: OPHTEC BV
• Contact Address: Schweitzerlaan 15 ; Groningen NL-GR Groningen 9728 NL
• US Agent:
  • Abraham Farhan
  • OPHTEC USA, INC.
  • 877 2042275 0
  • 877 7665447
  • abraham.farhan@usa.ophtec.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Sawgrass Executive Center 400 Sawgrass Corporate Pkwy, Suite 220; Sunrise, FL 33325 US
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMN P030023 | MRJ Abraham Farhan [OPHTEC BV]	StabilEyes Capsular Tension Ring	2007-12-05
PMN P030023 | MRJ Abraham Farhan [OPHTEC BV]	RingJect	2007-12-05
PMN P030023 | MRJ Abraham Farhan [OPHTEC BV]	Ophtec Capsular Tension Ring	2007-12-05
PMN K030471 | HNQ Abraham Farhan [OPHTEC BV]	Verisyse - Veriflex Enclavation Needle	2007-12-05
PMN K030471 | HNQ Abraham Farhan [OPHTEC BV]	Artisan - Artiflex Enclavation Needle	2007-12-05
PMN K011498 | NCE Abraham Farhan [OPHTEC BV]	StablEyes Capsular Tension Ring Inserter	2007-12-05
PMN K011498 | NCE Abraham Farhan [OPHTEC BV]	Easy Control Micro Inserter	2007-12-05
PMN P030028 | MTA Abraham Farhan [OPHTEC BV]	Verisyse Myopia Phakic Lens	2004-12-15
PMN P030028 | MTA Abraham Farhan [OPHTEC BV]	Veriflex Myopia Phakic Lens	2004-12-15
PMN P030028 | MTA Abraham Farhan [OPHTEC BV]	Artisan Myopia Phakic Lens	2004-12-15
PMN P030028 | MTA Abraham Farhan [OPHTEC BV]	Artiflex Myopia Phakic Lens	2004-12-15

Similar & Related FDA Registered Companies

• OPHTEC USA, INC.