Data / Medical devices / Restoration, Porcelain / United States
FDA-registered makers of Restoration, Porcelain in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Restoration, Porcelain (product code NSP). 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
- Restoration, Porcelain
- Product code
- NSP
- Country
- United States
Makers of Restoration, Porcelain in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Fortis Dental Lab | Bradenton, FL, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Implant Solutions Pty Ltd (trading AS Osteon Medical) | Irvine, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kelsey Dental LLC | The Woodlands, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KTJ Dental Lab Inc | Los Angeles, CA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Laxmi Dental Lab Usa Inc. | Kenilworth, NJ, United States | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Perfect Crown Dental Lab | Maspeth, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Preferred Dental Laboratory, Inc. | Roseland, NJ, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| United Laboratories Corporation | Tukwila, WA, 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.