Dual Top Screw System— 510(k) K161335

Substantially Equivalent

Jeil Medical Corporation

FDA 510(k) clearance K161335 for Dual Top Screw System, Substantially Equivalent on 2017-02-23. Applicant: Jeil Medical Corporation.

Clearance details

Applicant: Jeil Medical Corporation
Product code: Code OAT
Advisory panel: Dental
Date received: 2016-05-12
Decision date: 2017-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seoul, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code OAT

product code OAT

Injury: 355
Total: 355

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.