Alcresta Therapeutics, Inc. - FDA 510(k) Cleared Devices
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) cleared devices by Alcresta Therapeutics, Inc.
7 devices
Cleared
Apr 17, 2025
RELiZORB (100300/100301)
Gastroenterology & Urology
56d
Cleared
Jan 15, 2025
RELiZORB (100300/ 100301)
Gastroenterology & Urology
90d
Cleared
Dec 21, 2023
RELiZORB®
Gastroenterology & Urology
101d
Cleared
Aug 30, 2023
Enzyme Packed Cartridge - RELiZORB
Gastroenterology & Urology
128d
Cleared
Dec 04, 2019
RELiZORB
Gastroenterology & Urology
195d
Cleared
Jul 12, 2017
Relizorb
Gastroenterology & Urology
253d
Cleared
Jun 30, 2016
Relizorb
Gastroenterology & Urology
58d