Data / Medical devices / United States / The TOVA Company
The TOVA Company: FDA-registered device maker in Langley, WA, United States, 1 510(k) clearance
The TOVA Company is registered with the FDA (registration 3015345316) in Langley, WA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 22, 2018. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3015345316
- Address
- 222 Anthes Ave Ste 101, Langley, WA, United States, 98260
- Owner or operator
- The TOVA Company (10056453)
- Roles
- Manufacturer
- First device listed
- December 27, 2018
- Registered through
- 2027
- Brand names listed
- Test of Variables of Attention (T.O.V.A.)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Recorder, Attention Task Performance | LQD | U | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 22, 2018 | K173915 | Test of Variables of Attention (T.O.V.A.) | LQD | Substantially Equivalent | The Tova Company | accessdata.fda.gov |
Compare with other makers
Updated March 22, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.