Galvanize Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Galvanize Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aliya® EX System, INUMI™ Flex Needle, Aliya(TM) System, Aliya(TM) Generator, Aliya(TM) Needle, Aliya(TM) Electrode
3
Total
3
Cleared
0
Denied
Galvanize Therapeutics, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Carlos, US.
Latest FDA clearance: May 2026. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Galvanize Therapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DuVal & Associates, P.A. as regulatory consultant.
FDA 510(k) Regulatory Record - Galvanize Therapeutics, Inc.
3 devices