LAKONG ULTRASONIC SCALER— 510(k) K103498

Name: FDA 510(k) clearance K103498
Creator: U.S. Food and Drug Administration
Published: 2011-03-31

Substantially Equivalent

Lakong Medical Device Company, Ltd.

FDA 510(k) clearance K103498 for LAKONG ULTRASONIC SCALER, Substantially Equivalent on 2011-03-31. Applicant: Lakong Medical Device Company, Ltd.. Device class: 2.

Clearance details

Applicant: Lakong Medical Device Company, Ltd.
Product code: Code ELC
Device class: Class 2
Regulation: 21 CFR 872.4850
Advisory panel: Dental
Date received: 2010-11-29
Decision date: 2011-03-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: City Of Industry, CA, 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.