K911271Substantially Equivalent
Adhesive Precoated Brackets
Unitek Corp., Monrovia CA / Traditional, Substantially Equivalent
K911271 is the FDA 510(k) clearance record for ADHESIVE PRECOATED BRACKETS, a class II device, cleared for Unitek Corp. on under FDA product code DYH (Adhesive, Bracket And Tooth Conditioner, Resin). FDA records list 23 510(k) clearances for Unitek Corp., from to . As of , FDA records show no recalls naming K911271.
Clearance record
- Decision date
- Received
- (68 days to decision)
- Product code
- DYH Adhesive, Bracket And Tooth Conditioner, Resin
- Regulation
- 21 CFR 872.3750
- Device class
- Class II
- Review panel
- Dental
- Applicant
- Unitek Corp. 2724 S. Peck Rd., Monrovia CA
- Third party review
- No
Clearances, product code DYH
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 | 1 |
| 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.
