VITRON M— 510(k) K990763

Substantially Equivalent

Espe Dental AG

FDA 510(k) clearance K990763 for VITRON M, Substantially Equivalent on 1999-05-25. Applicant: Espe Dental AG.

Clearance details

Applicant: Espe Dental AG
Product code: Code EBI
Advisory panel: Dental
Date received: 1999-03-08
Decision date: 1999-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bavaria D-82228 Seefeld, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code EBI

product code EBI

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.