
Iop, Inc.
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MODIFIED MOLTENO(TM) IMPLANTS is an FDA 510(k)-cleared medical device (K902489) manufactured by Iop, 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 August 13, 1990. Regulation: 8.

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