Wango Intl., Inc.
TaiwanFDA applicant, unverified
- Devices
- 1
What Wango Intl., Inc. makes
Wango Intl., Inc. manufactures patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves Ref K892505
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wango Intl., Inc. have in the registry?
The registry currently lists 1 device for Wango Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wango Intl., Inc.'s devices?
Among its 1 most recently registered device, Wango Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wango Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wango Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wango Intl., Inc. in the registry?
The most recently registered devices listed for Wango Intl., Inc. include PATIENT EXAMINATION GLOVES.