GRANDTEC— 510(k) K102347

Substantially Equivalent

Voco GmbH

FDA 510(k) clearance K102347 for GRANDTEC, Substantially Equivalent on 2010-10-29. Applicant: Voco GmbH.

Clearance details

Applicant: Voco GmbH
Product code: Code EBI
Advisory panel: Dental
Date received: 2010-08-19
Decision date: 2010-10-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cuxhaven, 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.