BONX805— 510(k) K243864

Substantially Equivalent

Bontech Co., Ltd.

FDA 510(k) clearance K243864 for BONX805, Substantially Equivalent on 2025-09-12. Applicant: Bontech Co., Ltd..

Clearance details

Applicant: Bontech Co., Ltd.
Product code: Code IZL
Advisory panel: Radiology
Date received: 2024-12-17
Decision date: 2025-09-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Suwon-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code IZL

product code IZL

Other: 3
Total: 3

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.