O2VENT T— 510(k) K161832

Substantially Equivalent

Oventus Manufacturing Pty, Ltd.

FDA 510(k) clearance K161832 for O2VENT T, Substantially Equivalent on 2016-09-23. Applicant: Oventus Manufacturing Pty, Ltd..

Clearance details

Applicant: Oventus Manufacturing Pty, Ltd.
Product code: Code LRK
Advisory panel: Dental
Date received: 2016-07-05
Decision date: 2016-09-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Indooroopilly, AU

Download summary PDF View on FDA.gov ↗

Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

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.