
Herniamesh S.R.L.
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RELIMESH is an FDA 510(k)-cleared medical device (K081327) manufactured by Herniamesh S.R.L.. 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 June 18, 2008. Regulation: 8.