INTERPLAK— 510(k) K852476

Substantially Equivalent

Dental Research Corp.

FDA 510(k) clearance K852476 for INTERPLAK, Substantially Equivalent on 1985-07-31. Applicant: Dental Research Corp..

Clearance details

Applicant: Dental Research Corp.
Product code: Code JEQ
Advisory panel: Dental
Date received: 1985-06-11
Decision date: 1985-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucker, GA, US

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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.