SurgiLance® Safety Lancet— 510(k) K222224

Substantially Equivalent

Medipurpose Pte. , Ltd.

FDA 510(k) clearance K222224 for SurgiLance® Safety Lancet, Substantially Equivalent on 2022-09-22. Applicant: Medipurpose Pte. , Ltd..

Clearance details

Applicant: Medipurpose Pte. , Ltd.
Product code: Code FMK
Advisory panel: General, Plastic Surgery
Date received: 2022-07-25
Decision date: 2022-09-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Singapore, SG

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.