Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled 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 Dynavox and its 2 subsidiaries with 6 device recalls. The most recent is a device recall dated Jan 14, 2013: P10 Tobii battery box (product number 510410) Product Usage - Battery pack for MyTobi….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Tobii Dynavox and its 2 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| 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
