Dutch Ophthalmic Usa Inc

FDA Filings

This page includes the latest FDA filings for Dutch Ophthalmic Usa Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number1222074
FEI Number3007916166
NameDUTCH OPHTHALMIC USA, INC.
Owner & OperatorDUTCH OPHTHALMIC USA, INC.
Contact Address10 Continental Drive, Bldg. 1
Exeter NH 03833 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address10 CONTINENTAL DRIVE BUILDING 1
Exeter, NH 03833 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
DUTCH OPHTHALMIC USA, INC.
Keratoprosthesis2013-09-19
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. CRYOSTAR CRYOSURGICAL SYSTEM2001-10-22
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. HARMONY TOTAL TTC VITRECTOMY SYSTEM2001-03-12
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. HARMONY TOTAL VITRECTOMY SYSTEM1999-03-03
DUTCH OPHTHALMIC USA, INC.
FIBER OPTIC ENDOILLUMINATION PROBE1998-05-20
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. HEXON ILLUMINATION SYSTEM1997-11-25
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. SOLUX LIGHT SOURCE1997-11-07
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. MICRODIATHERMY SYSTEM1996-08-29
DUTCH OPHTHALMIC USA, INC.
D.O.R.C. VFI/VFE SYSTEM1996-04-15
DUTCH OPHTHALMIC USA, INC.
OPHTHALMIC CRYO UNIT1994-07-18
DUTCH OPHTHALMIC USA, INC.
ECKHARDT TEMPORARY KERATOPROSTHESIS1990-06-26

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