Skip to content

Annabella, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Annabella, Ltd. makes

Annabella, Ltd. manufactures the Annabella Breast Pump, a device designed for lactating individuals to express milk manually or electrically.

The breast pump is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Annabella Breast Pump Ref K230672

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Annabella, Ltd. have in the registry?

The registry currently lists 1 device for Annabella, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Annabella, Ltd.'s devices?

Among its 1 most recently registered device, Annabella, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Annabella, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Annabella, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Annabella, Ltd. in the registry?

The most recently registered devices listed for Annabella, Ltd. include Annabella Breast Pump.

Generated automatically from registry data and not verified by a human reviewer.