OssBuilder System— 510(k) K172354

Substantially Equivalent

Osstem Implant Co., Ltd.

FDA 510(k) clearance K172354 for OssBuilder System, Substantially Equivalent on 2018-03-26. Applicant: Osstem Implant Co., Ltd..

Clearance details

Applicant: Osstem Implant Co., Ltd.
Product code: Code JEY
Advisory panel: Dental
Date received: 2017-08-03
Decision date: 2018-03-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Busan, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code JEY

product code JEY

Injury: 1,542
Malfunction: 2,292
Total: 3,834

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.