Medical Device Manufacturer · US , Newton , MA

Alcresta Therapeutics, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2016

Recent clearances: RELiZORB (100300/100301), RELiZORB (100300/ 100301), RELiZORB®

7
Total
7
Cleared
0
Denied

Alcresta Therapeutics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Newton, US.

Latest FDA clearance: Apr 2025. Active since 2016. Primary specialty: Gastroenterology & Urology.

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

FDA 510(k) Regulatory Record - Alcresta Therapeutics, Inc.

7 devices
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