Medical Device Manufacturer · IT , Florence

Mattioli Engineering, Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mattioli Engineering, Srl General & Plastic Surgery ✕

2 devices

1-2 of 2

Cleared Dec 09, 1996

DMS-1000C DERMOABRADER

General & Plastic Surgery · 115d

Cleared Dec 15, 1994

MULTIPLE CO2 LAERS

General & Plastic Surgery · 246d

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 28, 2026