MERIDIEN DENTAL SYSTEMS— 510(k) K903488

Substantially Equivalent

Anco Merchandise Co., Ltd.

FDA 510(k) clearance K903488 for MERIDIEN DENTAL SYSTEMS, Substantially Equivalent on 1991-07-09. Applicant: Anco Merchandise Co., Ltd..

Clearance details

Applicant: Anco Merchandise Co., Ltd.
Product code: Code JEQ
Advisory panel: Dental
Date received: 1990-08-01
Decision date: 1991-07-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, Taiwan, R.O.C., CN

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Adverse events under product code JEQ

product code JEQ

Injury: 188
Malfunction: 2,818
Total: 3,006

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.