# Mattioli Engineering Corp.

- Location (FDA's records): Florence, IT
- FDA decisions: 5 (1994–2010): 5 510(k) clearances
- Names in FDA's records: Mattioli Engineering Corp. (3); Mattioli Engineering, Srl (2)
- Product codes: EGJ (2), GFD (1), ONF (1), GEX (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 6 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Life-Tech Intl., Inc.: 2 (https://510kreport.com/company/life-tech-intl)

## Firms that cite its devices most
- Venus Concept, Ltd.: 2 (https://510kreport.com/company/venus-concept)
- Aa Advanced Technology, Inc.: 2 (https://510kreport.com/company/aa-advanced-technology)
- Iomed, Inc.: 1 (https://510kreport.com/company/iomed)

## Its most-cited devices
- K100053: Mattioli Pulse Two/Three Plus Family (2010), cited by 2
- K032968: Trsansderm Ionto System (2003), cited by 2
- K042590: Transderm Ionto System, MK 2 (2004), cited by 2

## Recent decisions
- K100053: Mattioli Pulse Two/Three Plus Family (Mar 10, 2010)
- K042590: Transderm Ionto System, MK 2 (Oct 14, 2004)
- K032968: Trsansderm Ionto System (Dec 2, 2003)
- K965256: DMS-1000C Dermoabrader (Dec 9, 1996)
- K941838: Multiple CO2 Laers (Dec 15, 1994)

Source page: https://510kreport.com/company/mattioli-engineering