Data / Medical devices / Light, Operating, Dental / United States
FDA-registered makers of Light, Operating, Dental in the United States: 18 establishments
18 establishments in the United States are registered with the FDA to make Light, Operating, Dental (product code EAZ). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Light, Operating, Dental
- Product code
- EAZ
- Country
- United States
Makers of Light, Operating, Dental in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| A-dec, Inc. | Newberg, OR, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 1 | July 14, 1989 | 0 | 0 | 0 | api.fda.gov |
| Den-Mat Holdings, LLC | Lompoc, CA, United States | Complaint file establishment, Specification developer | 1 | November 22, 2004 | 0 | 0 | 0 | api.fda.gov |
| Summit Dental Systems LLC. | Fort Lauderdale, FL, United States | Manufacturer | 1 | September 29, 1986 | 0 | 0 | 0 | api.fda.gov |
| Addent, Inc. | Danbury, CT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ascentcare Dental Products | Grand Haven, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aseptico, Inc. | Woodinville, WA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Beaverstate Dental, Inc. | Newberg, OR, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| DCI International, LLC | Newberg, OR, United States | Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Dental Technologies, Inc. | Lincolnwood, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentalez Of Alabama | Bay Minette, AL, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dexta Corp. | Napa, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dntlworks Equipment Corp. | Centennial, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ergonomic Products, Inc. | Fall River, MA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Forest Dental Equipment | Bay Minette, AL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mastercraft Dental Co. Of Texas | Midlothian, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Midmark Corporation | Versailles, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Oralkleen LLC | Phoenix, AZ, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Proma, Inc. | Carson, CA, United States | 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.