Avent America, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
Avent Nipple Shield Ref K944117
510(k) 510(k)Niplette Ref K952035
510(k) 510(k)
Frequently asked questions
How many devices does Avent America, Inc. have in the registry?
The registry currently lists 4 devices for Avent America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Avent America, Inc.'s devices?
Among its 4 most recently registered devices, Avent America, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Avent America, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Avent America, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Avent America, Inc. in the registry?
The most recently registered devices listed for Avent America, Inc. include ISIS IQ UNO HANDHELD ELECTRONIC BREAST PUMP, MODEL 101, ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100, AVENT NIPPLE SHIELD and NIPLETTE.