Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Therabody with 2 510(k) clearances and 1 device recall. The most recent is a device recall dated Jun 23, 2026: Charger for the Therabody Theragun, G4 PRO massage device, and products which include th….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jun 23, 2026 | Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO BlaClass II · Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of therm | Device recalls |
| Aug 30, 2024 | JetBoots PRO PlusK241256 · IRP | 510(k) clearances |
| Jun 9, 2023 | TheraFace MaskK230293 · OHS | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
