Data / Medical devices / Hearing Aid, Air-Conduction, Over The Counter / United States
FDA-registered makers of Hearing Aid, Air-Conduction, Over The Counter in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Hearing Aid, Air-Conduction, Over The Counter (product code QUF). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Hearing Aid, Air-Conduction, Over The Counter
- Product code
- QUF
- Country
- United States
Makers of Hearing Aid, Air-Conduction, Over The Counter in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aha Technologies, Inc. | Detroit, MI, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Audicon Corporation | Ontario, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Audition Technology | Chicago, IL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Etymotic Research, Inc. | Schaumburg, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ga Trading LLC | Cheyenne, WY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hearing Lab Technology, LLC | Fort Worth, TX, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hearing Lab Technology, LLC. | West Bristol, PA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jlab | Carlsbad, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MDHearing Warehouse | Chicago, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Magnatone Hearing Aid Corp. dba Persona Medical | Casselberry, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novidan, Inc. | Golden Valley, MN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.