Data / Medical devices / Dental Abutment Design Software For Dental Laboratory / United States
FDA-registered makers of Dental Abutment Design Software For Dental Laboratory in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Dental Abutment Design Software For Dental Laboratory (product code PNP). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Dental Abutment Design Software For Dental Laboratory
- Product code
- PNP
- Country
- United States
Makers of Dental Abutment Design Software For Dental Laboratory in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Prismatik Dentalcraft, Inc. | Irvine, CA, United States | Complaint file establishment, Manufacturer | 1 | March 14, 2024 | 0 | 0 | 0 | api.fda.gov |
| Biohorizons Implant Systems Inc. | Birmingham, AL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Creodent Hudson Valley | Fishkill, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Implant Direct Sybron Manufacturing LLC | Thousand Oaks, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Implant Logistics / AMS Micromedical | Sparta, WI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micro Precision Swiss | Santa Ana, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| New Image Dental Laboratory, Inc. | Morrow, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nobel Biocare Procera, LLC | Mahwah, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Nobel Biocare Usa, LLC | Yorba Linda, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PREAT Corporation | Santa Maria, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Straumann Manufacturing, Inc. | Mansfield, TX, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Straumann Manufacturing, Inc. | Andover, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.