Data / Medical devices / Unit, X-Ray, Extraoral With Timer / United States
FDA-registered makers of Unit, X-Ray, Extraoral With Timer in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Unit, X-Ray, Extraoral With Timer (product code EHD). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Unit, X-Ray, Extraoral With Timer
- Product code
- EHD
- Country
- United States
Makers of Unit, X-Ray, Extraoral With Timer in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Dental Imaging Technologies Corporation | Quakertown, PA, United States | Complaint file establishment, Manufacturer | 2 | March 20, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ads Dental System Inc. | Ontario, CA, United States | Remanufacturer | 1 | March 12, 2026 | 0 | 0 | 0 | api.fda.gov |
| Livermoretech,inc | Plano, TX, United States | Manufacturer | 1 | December 19, 2019 | 0 | 0 | 0 | api.fda.gov |
| Lucas Lifecare, LLC | Janesville, WI, United States | Manufacturer | 1 | July 5, 2024 | 0 | 0 | 0 | api.fda.gov |
| Midmark Corporation | Versailles, OH, United States | Manufacturer | 1 | December 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| Valkyrie Bioscience, Inc | Lindon, UT, United States | Complaint file establishment, Specification developer | 1 | July 6, 2023 | 0 | 0 | 0 | api.fda.gov |
| Dentsply LLC | York, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Turner Imaging Systems, Inc. | Orem, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.