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Biomet, Inc.
Free shipping on orders over $99 · 30-day returns
LORENZ LACTOSORB VOCAL MEDIALIZATION IMPLANT is an FDA 510(k)-cleared medical device (K011554) manufactured by Biomet, Inc.. This device is classified under the Ear, Nose, Throat specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 25, 2001. Regulation: 8.

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