Contact Lens Loupe, Inspetion Loupe

No FDA recalls found in the data synced 10 Oct 2026.

510(k) Number

K852054 ↗

FDA Product Code

HLN

Device Class

Class I

Regulation

21 CFR Part 886.1420

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

• Atf 101 Trail Frame

  Class I

  FDA 510(k) K852126 Active Cleared 5 Jun 1985

• Atl 225 Mw Trail Lens Set

  Class I

  FDA 510(k) K852548 Active Cleared 31 Jul 1985

• Ascon Ophthalmic Sponge

  Class II

  FDA 510(k) K852055 Active Cleared 4 Sep 1985

• Acc Cross Cylinders

  Class I

  FDA 510(k) K852056 Active Cleared 5 Jun 1985

• Ascon Surgical Instruments

  Class I

  FDA 510(k) K852057 Active Cleared 27 Jun 1985