Oneday Mini Implant System— 510(k) K222946

Substantially Equivalent

Oneday Biotech Co., Ltd.

FDA 510(k) clearance K222946 for Oneday Mini Implant System, Substantially Equivalent on 2023-08-23. Applicant: Oneday Biotech Co., Ltd..

Clearance details

Applicant: Oneday Biotech Co., Ltd.
Product code: Code DZE
Advisory panel: Dental
Date received: 2022-09-27
Decision date: 2023-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Daegu, KR

Download summary PDF View on FDA.gov ↗

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.