Product code NDP— Dental
CEREC Guides
- Classification name
- Accessories, Implant, Dental, Endosseous
- Device class
- Class 1
- Regulation
- 21 CFR 872.3980
- Advisory panel
- Dental
- Total cleared
- 4
- First cleared
- Most recent
Market context for product code NDP
FDA has cleared devices under product code NDP between 2007 and 2020, filed by 2 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 2020
- 2019
- 2017
- 2007
Top applicants under product code NDP
Adverse events under product code NDP
product code NDP- Injury
- 454
- Malfunction
- 1,956
- Total
- 2,410
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code NDP
Data sourced from openFDA. This site is unofficial and independent of the FDA.