Sterilized Eol Auto Lancet; Sterilized Eol Lancet Plus— 510(k) K243533

Substantially Equivalent

Hlb Co., Ltd. Healthcare

FDA 510(k) clearance K243533 for Sterilized Eol Auto Lancet; Sterilized Eol Lancet Plus, Substantially Equivalent on 2025-01-13. Applicant: Hlb Co., Ltd. Healthcare.

Clearance details

Applicant: Hlb Co., Ltd. Healthcare
Product code: Code FMK
Advisory panel: General, Plastic Surgery
Date received: 2024-11-15
Decision date: 2025-01-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sejong-Si, KR

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMK

product code FMK

Injury: 133
Malfunction: 1,278
Other: 1
Total: 1,412

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.