
Meditrade, Inc.
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MEDITRADE ARTIFICIAL EYES AND IMPLANTS is an FDA 510(k)-cleared medical device (K862977) manufactured by Meditrade, Inc.. This device is classified under the Ophthalmic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 19, 1986. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280