Domino S.R.L.
Country not established FDA
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Domino S.R.L. makes
Domino S.R.L. manufactures external neuromuscular electrical stimulators, including the Globus Genesy 1100 Stimulator and the Globus Premium Muscle Stimulator, designed for therapeutic muscle activation and rehabilitation.
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
Globus Genesy 1100 Stimulator Ref K071431
510(k) 510(k)Globus Premium Muscle Stimulator Ref K061632
510(k) 510(k)
FDA establishments
- Domino S.R.L. Codogne Treviso · IT FEI 3006153348
Frequently asked questions
How many devices does Domino S.R.L. have in the registry?
The registry currently lists 2 devices for Domino S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Domino S.R.L.'s devices?
Among its 2 most recently registered devices, Domino S.R.L. has devices listed in FDA 510(k) (2 devices).
What risk classes do Domino S.R.L.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Domino S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Domino S.R.L. in the registry?
The most recently registered devices listed for Domino S.R.L. include GLOBUS GENESY 1100 STIMULATOR and GLOBUS PREMIUM MUSCLE STIMULATOR.
Which FDA establishments are linked to Domino S.R.L.?
1 FDA establishment is linked to Domino S.R.L. in the registry; they are listed on the company page.