D.O.R.C. Vfi/Vfe System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K954842 ↗

FDA Product Code

KYG

Device Class

Class I

Regulation

21 CFR Part 886.4360

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• D.O.R.C. Hexon Illumination System

  Class II

  FDA 510(k) K973229 Active Cleared 25 Nov 1997

• D.O.R.C. Microdiathermy System

  Class II

  FDA 510(k) K962135 Active Cleared 29 Aug 1996

• D.O.R.C. Solux Light Source

  Class II

  FDA 510(k) K973757 Active Cleared 7 Nov 1997

• D.O.R.C. CryoStar Cryosurgical System

  Class II

  FDA 510(k) K012821 Active Cleared 22 Oct 2001

• Fiber Optic Endoillumination Probe

  Class II

  FDA 510(k) K980636 Active Cleared 20 May 1998

• D.O.R.C. Harmony Total Ttc Vitrectomy System

  Class II

  FDA 510(k) K010082 Active Cleared 12 Mar 2001

See all devices from Dutch Ophthalmic USA, Inc. →