Trilogy Tissue Marker— 510(k) K240429

Substantially Equivalent

Inrad, Inc.

FDA 510(k) clearance K240429 for Trilogy Tissue Marker, Substantially Equivalent on 2024-11-07. Applicant: Inrad, Inc..

Clearance details

Applicant: Inrad, Inc.
Product code: Code NEU
Advisory panel: General, Plastic Surgery
Date received: 2024-02-13
Decision date: 2024-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kentwood, MI, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code NEU

product code NEU

Injury: 824
Total: 824

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.