DIJI-DENT— 510(k) K781962

Substantially Equivalent

J&J Technologies, Inc.

FDA 510(k) clearance K781962 for DIJI-DENT, Substantially Equivalent on 1978-12-20. Applicant: J&J Technologies, Inc..

Clearance details

Applicant: J&J Technologies, Inc.
Product code: Code EFW
Advisory panel: Dental
Date received: 1978-11-21
Decision date: 1978-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code EFW

product code EFW

Injury: 143
Malfunction: 698
Total: 841

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.