LORENZ INTRAORAL LINEAR MANDIBULAR DISTRACTION SYSTEM— 510(k) K982906

Substantially Equivalent

Walter Lorenz Surgical, Inc.

FDA 510(k) clearance K982906 for LORENZ INTRAORAL LINEAR MANDIBULAR DISTRACTION SYSTEM, Substantially Equivalent on 1998-11-12. Applicant: Walter Lorenz Surgical, Inc..

Clearance details

Applicant: Walter Lorenz Surgical, Inc.
Product code: Code MQN
Advisory panel: Dental
Date received: 1998-08-18
Decision date: 1998-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jacksonville, FL, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MQN

product code MQN

Injury: 346
Total: 346

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.