Medical Device Manufacturer · US , Burlingame , CA

Neptune Medical, Inc. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 2019
5
Total
4
Cleared
0
Denied

Neptune Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Burlingame, US.

Latest FDA clearance: Jun 2024. Active since 2019. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by AlvaMed, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Neptune Medical, Inc.
5 devices
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