Claritag Advanced— 510(k) K222356

Substantially Equivalent

Dgi Technologies

FDA 510(k) clearance K222356 for Claritag Advanced, Substantially Equivalent on 2023-05-18. Applicant: Dgi Technologies.

Clearance details

Applicant: Dgi Technologies
Product code: Code GEH
Advisory panel: General, Plastic Surgery
Date received: 2022-08-04
Decision date: 2023-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Howell, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEH

product code GEH

Death: 25
Injury: 351
Malfunction: 901
Total: 1,277

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.