
Lsi Solutions, Inc.
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MD Mattress Suture Placement Device is an FDA 510(k)-cleared medical device (K222783) manufactured by Lsi Solutions, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 11, 2024. Regulation: 8.