ENDO-EZE MOTOR AND HANDPIECE— 510(k) K992380

Substantially Equivalent

Ultradent Products, Inc.

FDA 510(k) clearance K992380 for ENDO-EZE MOTOR AND HANDPIECE, Substantially Equivalent on 1999-10-13. Applicant: Ultradent Products, Inc.. Device class: 1.

Clearance details

Applicant
Ultradent Products, Inc.
Product code
Code EFB
Device class
Class 1
Regulation
21 CFR 872.4200
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
South Jordan, UT, US
Download summary PDFView on FDA.gov ↗

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Adverse events under product code EFB

product code EFB
Injury
133
Malfunction
562
Total
695

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.