Pharmaceutical companyLabelled 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 its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list TheraTech, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 10, 2006: IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2.
| Date | Record | Source |
|---|---|---|
| May 10, 2006 | IF TRUE SINE INTERFERENTIAL STIMULATOR / MODEL WL-2206A1 & WI-2206A2K060975 · LIH | 510(k) clearances |
| Jun 17, 2005 | IF TRUE SINE INTERFERENTIAL STIMULATOR, MODEL WL-2206AK050847 · IPF | 510(k) clearances |
| Feb 25, 2003 | IF SERIES TRUE SINE INTERFERENTIAL STIMULATOR/MODEL: WL-2206, WELL IF, LIFE IF AND THE CUSTOMER PRIVATE BRANDK024100 · LIH | 510(k) clearances |
| Jul 30, 2002 | TTECH MODEL 200E + TENS DEVICEK021436 · GZJ | 510(k) clearances |
| Jul 3, 2002 | POWERED MUSCLE STIMULATORK013768 · IPF | 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
