Data / Medical devices / Articulators / United States
FDA-registered makers of Articulators in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Articulators (product code EJP). 0 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
- Articulators
- Product code
- EJP
- Country
- United States
Makers of Articulators in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advanced Dental Designs | Moreno Valley, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Asap LLC | Santa Fe Spgs, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Buffalo Dental MFG. Co., Inc. | Syosset, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentsply LLC | York, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Keystone Industries | Myerstown, PA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Myotronics-Noromed, Inc. | Kent, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Panadent Corp. | Colton, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Premier Dental Products Co. | Plymouth Meeting, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prismatik Dentalcraft, Inc. | Irvine, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reko Dental, LLC | Gardena, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Whip-Mix Corp. | Louisville, KY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| World Lab U.S.A. | Irvine, CA, United States | Manufacturer for export | 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.