Data / Medical devices / United States / Ear Technology Corporation
Ear Technology Corporation: FDA-registered device maker in Johnson City, TN, United States, 1 510(k) clearance
Ear Technology Corporation is registered with the FDA (registration 1056339) in Johnson City, TN, United States. It lists 6 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 8, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1056339
- FEI number
- 1000140463
- Address
- 106 E Watauga Ave., Johnson City, TN, United States, 37601
- Owner or operator
- EAR TECHNOLOGY CORPORATION (9007312)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- March 26, 1993
- Registered through
- 2026
- Brand names listed
- Breeze by Dry&Store, Clik, Dry Brik II, Dry Caddy by Dry&Store, Dry Disc by Dry&Store, Dry&Store Global II, Dry-Brik by Dry&Store, DryBoost and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Curette, Ear | JYG | 1 | Specification developer | accessdata.fda.gov |
| Disinfector, Medical Devices | MEC | 2 | Specification developer | accessdata.fda.gov |
| Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter | QUG | 2 | Repackager or relabeler | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Over The Counter | QUF | 1 | Repackager or relabeler | accessdata.fda.gov |
| Hearing Aid, Air-Conduction, Prescription | ESD | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Instrument, Ent Manual Surgical | LRC | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| September 8, 1997 | K972776 | DRY & STORE | ESD | Substantially Equivalent | Ear Technology Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Hearing Aid, Air-Conduction, Prescription
- All makers of Instrument, Ent Manual Surgical
- All makers of Curette, Ear
- All makers of Disinfector, Medical Devices
- All makers of Hearing Aid, Air-Conduction, Over The Counter
- All makers of Hearing Aid, Air-Conduction With Wireless Technology, Over The Counter
Updated September 8, 1997. 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.