Laser Dock— 510(k) K152636

Substantially Equivalent

Patient Pocket, LLC

FDA 510(k) clearance K152636 for Laser Dock, Substantially Equivalent on 2015-12-17. Applicant: Patient Pocket, LLC.

Clearance details

Applicant: Patient Pocket, LLC
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2015-09-15
Decision date: 2015-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cherry Hill, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.