Mectronic Medicale S.r.l.
ItalyFDA applicant, unverified FDA FEI 3015283772
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Mectronic Medicale S.r.l. makes
Mectronic Medicale S.R.L. manufactures Tecar therapy devices, including the Doctor Tecar Plus and Doctor Tecar Smart, which are designed for soft tissue treatment and regenerative medicine applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Doctor Tecar Plus, Doctor Tecar Smart Ref K221043
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015283772
- Address
- Via Orio al Serio, 15, Grassobbio Bergamo
Frequently asked questions
How many devices does Mectronic Medicale S.R.L. have in the registry?
The registry currently lists 1 device for Mectronic Medicale S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mectronic Medicale S.R.L.'s devices?
Among its 1 most recently registered device, Mectronic Medicale S.R.L. has devices listed in FDA 510(k) (1 device).
What risk classes do Mectronic Medicale S.R.L.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mectronic Medicale S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mectronic Medicale S.R.L. in the registry?
The most recently registered devices listed for Mectronic Medicale S.R.L. include Doctor Tecar Plus, Doctor Tecar Smart.