DYNA TORQ TORQUE WRENCH, TORQUE WRENCH— 510(k) K991283

Name: FDA 510(k) clearance K991283
Creator: U.S. Food and Drug Administration
Published: 1999-08-18

Substantially Equivalent

Micro Motors, Inc.

FDA 510(k) clearance K991283 for DYNA TORQ TORQUE WRENCH, TORQUE WRENCH, Substantially Equivalent on 1999-08-18. Applicant: Micro Motors, Inc.. Device class: 2.

Clearance details

Applicant: Micro Motors, Inc.
Product code: Code DZE
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 1999-04-15
Decision date: 1999-08-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

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.