Data / Medical devices / Diagnostic Light, Soft Tissue Detector
Diagnostic Light, Soft Tissue Detector (NXV): 6 FDA-registered makers in 3 countries
6 establishments in 3 countries are registered with the FDA to make Diagnostic Light, Soft Tissue Detector (product code NXV, Class 2, 21 CFR 872.6350). 6 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on September 15, 2015, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- NXV
- Device class
- 2
- Regulation
- 872.6350
- Medical specialty
- Dental
Makers by country
| Country | Makers |
|---|---|
| United States | 4 |
| Canada | 1 |
| Italy | 1 |
Makers of Diagnostic Light, Soft Tissue Detector
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Den-Mat Holdings, LLC | Lompoc, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 2 | January 23, 2009 | 0 | 0 | 0 | api.fda.gov |
| Addent, Inc. | Danbury, CT, United States | Manufacturer | 1 | January 23, 2009 | 0 | 0 | 0 | api.fda.gov |
| Dentlight Inc. | Plano, TX, United States | Manufacturer | 1 | July 15, 2010 | 0 | 0 | 0 | api.fda.gov |
| Forward Science Technologies LLC | Houston, TX, United States | Manufacturer | 1 | March 13, 2013 | 0 | 0 | 0 | api.fda.gov |
| Led Dental Inc. | Vancouver British Columbia, Canada | Specification developer | 1 | November 18, 2010 | 0 | 0 | 0 | api.fda.gov |
| Pierrel S.P.A. | Capua Caserta, Italy | Repackager or relabeler, Specification developer | 1 | September 15, 2015 | 0 | 0 | 0 | api.fda.gov |
Updated September 15, 2015. 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.