Medical device makerLabelled 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 15, 2026, FDA's public records list Woodside Biomedical with 6 510(k) clearances. The most recent is a 510(k) clearance dated Mar 21, 2002: RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RL.
| Mar 21, 2002 | RELIEFBAND DEVICE, MODELS RB-DL, RB-EL, RB-RLK020180 · GZJ | 510(k) clearances |
| Mar 16, 2000 | RELIEFBAND NST DEVICE, MODEL WB-2L, WB-6L, WB-RLK994387 · GZJ | 510(k) clearances |
| Dec 9, 1999 | RELIEFBAND NST DEVICE MODELS WB-2,WB-6,WB-RK983907 · GZJ | 510(k) clearances |
| Feb 23, 1999 | RELIEFBAND MST DEVICE, MODELS RB-2, RB-6, RB-RK982967 · GZJ | 510(k) clearances |
| Oct 8, 1998 | RELIEFBAND NST DEVICE, MODEL #'S WB-2, WB-6 AND WB-RK982436 · GZJ | 510(k) clearances |
| Feb 18, 1998 | RELIEFBANDK980333 · GZJ | 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
