Sola Commido Loupe

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K760770 ↗

FDA Product Code

HLJ

Device Class

Class II

Regulation

21 CFR Part 886.1570

Advisory Committee

Ophthalmic

FDA Decision

SESE Substantially Equivalent

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• Orbit Galaxy G2 Microcoil Delivery System

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• Vanderbilt Pituitary Retractor

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• Codman Isocool Bipolar Forceps

  Class II

  FDA 510(k) K083895 Active Cleared 23 Jun 2009

See all devices from Codman & Shurtleff, Inc. →