Neomed, Inc. has 13 FDA 510(k) cleared medical devices. Based in Swanee, US.

Historical record: 13 cleared submissions from 2007 to 2019. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Neomed, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Neomed, Inc.

13 devices
1-12 of 13
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