Wb Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Wb Intl., Inc. makes
Wb Intl., Inc. makes cardiovascular balloon catheters and surgical gloves.
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Catheter, Cardiovascular, Balloon Type Ref K883852
Regimes: 510(k) Registry: 510(k)Surgical Gloves Ref K885089
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wb Intl., Inc. have in the registry?
The registry currently lists 2 devices for Wb Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wb Intl., Inc.'s devices?
Among its 2 most recently registered devices, Wb Intl., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Wb Intl., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Wb Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wb Intl., Inc. in the registry?
The most recently registered devices listed for Wb Intl., Inc. include CATHETER, CARDIOVASCULAR, BALLOON TYPE and SURGICAL GLOVES.