IMPLANTIUM PROSTHETICS— 510(k) K070228

Substantially Equivalent

Dentium Co., Ltd.

FDA 510(k) clearance K070228 for IMPLANTIUM PROSTHETICS, Substantially Equivalent on 2007-11-20. Applicant: Dentium Co., Ltd..

Clearance details

Applicant
Dentium Co., Ltd.
Product code
Code NHA
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Dunwoody, GA, US
Download summary PDFView on FDA.gov ↗

Adverse events under product code NHA

product code NHA
Injury
1,270
Malfunction
2,860
Total
4,130

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 →

Data sourced from openFDA. This site is unofficial and independent of the FDA.