Mattioli Engineering Corp.
Country not established
- Devices
- 5
What Mattioli Engineering Corp. makes
Mattioli Engineering Corp. manufactures transdermal iontophoresis systems, including the TRSANSDERM IONTO and TRANSDERM IONTO SYSTEM (MK 2), designed for drug delivery through the skin. The company also produces the MATTIOLI PULSE TWO/THREE PLUS family, which appears to include pulse-based medical devices for therapeutic applications.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Multiple CO2 Laers Ref K941838
Regimes: 510(k) Registry: 510(k)Mattioli Pulse Two/Three Plus Family Ref K100053
Regimes: 510(k) Registry: 510(k)Dms-1000C Dermoabrader Ref K965256
Regimes: 510(k) Registry: 510(k)Trsansderm Ionto System Ref K032968
Regimes: 510(k) Registry: 510(k)Transderm Ionto System, Mk 2 Ref K042590
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mattioli Engineering Corp. have in the registry?
The registry currently lists 5 devices for Mattioli Engineering Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mattioli Engineering Corp.'s devices?
Among its 5 most recently registered devices, Mattioli Engineering Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Mattioli Engineering Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Mattioli Engineering Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mattioli Engineering Corp. in the registry?
The most recently registered devices listed for Mattioli Engineering Corp. include MULTIPLE CO2 LAERS, MATTIOLI PULSE TWO/THREE PLUS FAMILY, DMS-1000C DERMOABRADER and TRSANSDERM IONTO SYSTEM.