Golden Star SRL
ItalyFDA applicant, unverified FDA
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Golden Star SRL makes
Golden Star Srl manufactures the FISIOWARM 7.0, a medical device designed for physiotherapy applications, likely used for controlled thermal therapy or wound care.
The FISIOWARM 7.0 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Fisiowarm 7.0 Ref K232966
Regimes: 510(k) Registry: 510(k)
FDA establishments
- Golden Star Company Limited Quynh Phu District Thai Binh · VN FEI 3015491436
Frequently asked questions
How many devices does Golden Star Srl have in the registry?
The registry currently lists 1 device for Golden Star Srl. Devices recorded under merged duplicate company entries are counted once.
Which registries list Golden Star Srl's devices?
Among its 1 most recently registered device, Golden Star Srl has devices listed in FDA 510(k) (1 device).
What risk classes do Golden Star Srl's devices fall under?
Among its 1 most recently registered device, the classes recorded for Golden Star Srl's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Golden Star Srl in the registry?
The most recently registered devices listed for Golden Star Srl include FISIOWARM 7.0.
Which FDA establishments are linked to Golden Star Srl?
1 FDA establishment is linked to Golden Star Srl in the registry; they are listed on the company page.