Therabody, Inc

FDA Regulatory Profile

Therabody, Inc appears in FDA public data with 1 recall, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2835-2026, Class II) was initiated on June 23, 2026. Its most recent 510(k) clearance was granted on August 30, 2024.

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-2835-2026Class IICharger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th GeneraJune 23, 2026

Recent 510(k) Clearances

K-NumberDeviceDate
K241256JetBoots PRO PlusAugust 30, 2024
K230293TheraFace MaskJune 9, 2023