EMS PIEZON 707 BIK AND PIEZON 707 BIK LED— 510(k) K140990

Name: FDA 510(k) clearance K140990
Creator: U.S. Food and Drug Administration
Published: 2015-02-27

Substantially Equivalent

E.M.S Electro Medical Systems S.A

FDA 510(k) clearance K140990 for EMS PIEZON 707 BIK AND PIEZON 707 BIK LED, Substantially Equivalent on 2015-02-27. Applicant: E.M.S Electro Medical Systems S.A. Device class: 2.

Clearance details

Applicant: E.M.S Electro Medical Systems S.A
Product code: Code ELC
Device class: Class 2
Regulation: 21 CFR 872.4850
Advisory panel: Dental
Date received: 2014-04-17
Decision date: 2015-02-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marlborough, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code ELC

product code ELC

Malfunction: 1,255
Total: 1,255

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.