Theragun, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theragun, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TheraFace LED, RecoveryAir PRO, TheraFace Microcurrent
3
Total
3
Cleared
0
Denied
Theragun, Inc. has 3 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2021. Active since 2021.
Browse the FDA 510(k) cleared devices submitted by Theragun, 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 - Theragun, Inc.
3 devices