
Davol Inc., Sub. C. R. Bard, Inc.
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VENTRALIGHT ST MESH is an FDA 510(k)-cleared medical device (K101851) manufactured by Davol Inc., Sub. C. R. Bard, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 14, 2010. Regulation: 8.