Medical Device Manufacturer · US , Newburyport , MA

Neoseed Technology,Llc - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2002

Total

Cleared

Denied

Neoseed Technology,Llc has 1 FDA 510(k) cleared medical devices. Based in Newburyport, US.

Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Gastroenterology & Urology.

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

Neoseed Technology,Llc is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Neoseed Technology,Llc

1 devices

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