Medical Device Manufacturer · US , King Of Prussia , PA

Aspire Bariatrics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2018

Total

Cleared

Denied

Aspire Bariatrics, Inc. has 2 FDA 510(k) cleared medical devices. Based in King Of Prussia, US.

Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.

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

Aspire Bariatrics, Inc. 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 - Aspire Bariatrics, Inc.

2 devices

1-2 of 2