Data / Medical devices / Canada / Led Dental Inc.
Led Dental Inc.: FDA-registered device maker in Vancouver British Columbia, Canada, 1 510(k) clearance
Led Dental Inc. is registered with the FDA (registration 3005374252) in Vancouver British Columbia, Canada. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 18, 2010. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3005374252
- Address
- 997 Seymour St Suite 250, Vancouver British Columbia, Canada, V6B3M1
- Owner or operator
- LED DENTAL INC. (9077785)
- Roles
- Specification developer
- First device listed
- December 22, 2010
- Registered through
- 2026
- Brand names listed
- VELscope Mantis, VELscope Vx
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Diagnostic Light, Soft Tissue Detector | NXV | 2 | Specification developer | accessdata.fda.gov |
| Light, Examination, Medical, Battery Powered | KYT | 1 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 18, 2010 | K102083 | VELSCOPE VX | NXV | Substantially Equivalent | Led Dental, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Light, Examination, Medical, Battery Powered
- All makers of Diagnostic Light, Soft Tissue Detector
Updated November 18, 2010. 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.