
ETHICON, Inc.
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VYPRO MESH, VICRYL PROLENE PARTIALLY ABSORBABLE SYNTHETIC SURGICAL MESH is an FDA 510(k)-cleared medical device (K002672) manufactured by ETHICON, 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 November 21, 2000. Regulation: 8.