
Okapi Medical, LLC Dba Resivant Medical
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CUTIVA Topical Skin Adhesive (RM1700); CUTIVA PLUS Skin Closure System (RM1739) is an FDA 510(k)-cleared medical device (K250950) manufactured by Okapi Medical, LLC Dba Resivant Medical. 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 August 3, 2025. Regulation: 8.