
Baxter/ Synovis Micro Companies Alliance, Inc.
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Gem FlowCoupler System is an FDA 510(k)-cleared medical device (K190499) manufactured by Baxter/ Synovis Micro Companies Alliance, 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 September 5, 2019. Regulation: 8.