Gostar Co., Ltd.
TaiwanFDA applicant, unverified FDA FEI 3030626362
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Gostar Co., Ltd. makes
Gostar Co., Ltd. manufactures respiratory monitoring devices including the TD-7301 Peak Flow meter and TD-7301 Spirometer, as well as diabetic care products such as the TD-5010 Lancing Device and TD-5084 Sterile Lancets.
The company's products are classified as Class II medical devices and are listed in the FDA 510(k) registry. Gostar Co., Ltd. is based in the United States.
Catalogue
TD-7301 Peak Flow meter Ref K222810
Regimes: 510(k) Registry: 510(k)TD-7301 Spirometer (TD-7301) Ref K241843
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3030626362
- Address
- 2F., No. 65, Wuquan 7th Rd., Wugu Dist., New Taipei City
Frequently asked questions
How many devices does Gostar Co., Ltd. have in the registry?
The registry currently lists 3 devices for Gostar Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gostar Co., Ltd.'s devices?
Among its 3 most recently registered devices, Gostar Co., Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Gostar Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Gostar Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gostar Co., Ltd. in the registry?
The most recently registered devices listed for Gostar Co., Ltd. include TD-7301 Peak Flow meter, TD-7301 Spirometer (TD-7301) and TD-5010 Lancing Device and TD-5084 Sterile Lancets.