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., part of Tobii DynavoxLabelled 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 Tobii Assistive Technology with 1 device recall. The most recent is a device recall dated Jan 14, 2013: P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobi….
| Date | Record | Source |
|---|---|---|
| Jan 14, 2013 | P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobii P10 Device. MyTobii P10 is a portable eye-controlClass II · Tobii ATI customers P10 external battery pack, which contains sealed lead-acid batteries, malfunctioned while recharging | Device recalls |
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
