Gravitas Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gravitas Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Entarik NI Feeding Tube System, Entarik Feeding Tube System
2
Total
2
Cleared
0
Denied
Gravitas Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Nov 2024. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gravitas Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by RQM+ as regulatory consultant.
FDA 510(k) Regulatory Record - Gravitas Medical, Inc.
2 devices