DuoprossTM Smart Cap (Type I)— 510(k) K252518

Name: FDA 510(k) clearance K252518
Creator: U.S. Food and Drug Administration
Published: 2025-12-17

Substantially Equivalent

Duopross Meditech Corporate

FDA 510(k) clearance K252518 for DuoprossTM Smart Cap (Type I), Substantially Equivalent on 2025-12-17. Applicant: Duopross Meditech Corporate. Device class: 2.

Clearance details

Applicant: Duopross Meditech Corporate
Product code: Code FMF
Device class: Class 2
Regulation: 21 CFR 880.5860
Advisory panel: General Hospital
Date received: 2025-08-11
Decision date: 2025-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NY, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.