Data / Medical devices / United States / Anthrotronix, Inc.
Anthrotronix, Inc.: FDA-registered device maker in Silver Spring, MD, United States, 1 510(k) clearance
Anthrotronix, Inc. is registered with the FDA (registration 3008375586) in Silver Spring, MD, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 15, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008375586
- Address
- 8403 Colesville Rd Ste 1100, Silver Spring, MD, United States, 20910
- Owner or operator
- AnthroTronix, Inc. (10061127)
- Roles
- Manufacturer
- First device listed
- August 23, 2019
- Registered through
- 2026
- Brand names listed
- DANA
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 |
|---|---|---|---|---|---|---|
| October 15, 2014 | K141865 | DANA | LQD | Substantially Equivalent | Anthrotronix, Inc. | accessdata.fda.gov |
Compare with other makers
Updated October 15, 2014. 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.