Company · US

Mattioli Engineering Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 2010. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
EGJ	Device, Iontophoresis, Other Uses	2
GEX	Powered Laser Surgical Instrument	1
GFD	Dermatome	1
ONF	Powered Light Based Non-Laser Surgical Instrument With Thermal Effect	1

Decided	510(k)	Device and applicant	Code
Mar 10, 2010	K100053	MATTIOLI PULSE TWO/THREE PLUS FAMILY Mattioli Engineering Corp.	ONF
Oct 14, 2004	K042590	TRANSDERM IONTO SYSTEM, MK 2 Mattioli Engineering Corp.	EGJ
Dec 2, 2003	K032968	TRSANSDERM IONTO SYSTEM Mattioli Engineering Corp.	EGJ
Dec 9, 1996	K965256	DMS-1000C DERMOABRADER Mattioli Engineering, Srl, IT	GFD
Dec 15, 1994	K941838	MULTIPLE CO2 LAERS Mattioli Engineering, Srl, IT	GEX

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.