Therabody, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therabody, Inc. - FDA 510(k) Cleared Devices
Recent clearances: JetBoots PRO Plus, TheraFace Mask
2
Total
2
Cleared
0
Denied
Therabody, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Latest FDA clearance: Aug 2024. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Therabody, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Schiff & Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Therabody, Inc.
2 devices