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Bio-Med USA, Inc.
Free shipping on orders over $99 · 30-day returns
UNITOX BOTOX SYRINGE is an FDA 510(k)-cleared medical device (K123710) manufactured by Bio-Med USA, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 8, 2013. Regulation: 8.

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