Annabella Tech
IsraelFDA applicant, unverified FDA FEI 3029923636
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Annabella Tech makes
Annabella Tech manufactures the Annabella Double Breast Pump (ADO-US23-1000), a device designed for lactation support and milk expression.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
Annabella Double Breast Pump (ADO-US23-1000) Ref K241506
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3029923636
- Address
- 23/5 Hataas, Kfar Saba Central
Frequently asked questions
How many devices does Annabella Tech have in the registry?
The registry currently lists 3 devices for Annabella Tech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Annabella Tech's devices?
Among its 3 most recently registered devices, Annabella Tech has devices listed in FDA 510(k) (1 device) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Annabella Tech's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Annabella Tech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Annabella Tech in the registry?
The most recently registered devices listed for Annabella Tech include Annabella Breast Pump ANB-US23-1000, Annabella Double Breast Pump ADO-US23-1000 and Annabella Double Breast Pump (ADO-US23-1000).