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Biofilm, Inc.
Free shipping on orders over $99 · 30-day returns
EXAM ROOM ASTROGLIDE (PROFESSIONAL MARKET), TARGET LUBRICATING JELLY (OTC CONSUMER MARKET) is an FDA 510(k)-cleared medical device (K003867) manufactured by Biofilm, Inc.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 8, 2001. Regulation: 8.

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