K033697Substantially Equivalent
Power LED
Dental Products of USA, Inc., Miami FL / Traditional, Substantially Equivalent
K033697 is the FDA 510(k) clearance record for POWER LED, a class II device, cleared for Dental Products of USA, Inc. on under FDA product code EBZ (Activator, Ultraviolet, For Polymerization). FDA records list one 510(k) clearance for Dental Products of USA, Inc. As of , FDA records show no recalls naming K033697.
Clearance record
- Decision date
- Received
- (94 days to decision)
- Product code
- EBZ Activator, Ultraviolet, For Polymerization
- Regulation
- 21 CFR 872.6070
- Device class
- Class II
- Review panel
- Dental
- Applicant
- Dental Products of USA, Inc. 1460 NW 107 Ave., Suite G, Miami FL
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code EBZ
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 1 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
