Nixit Limited
Country not established FDA
Part of Nixit Limited
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Nixit Limited makes
Nixit Limited manufactures reusable menstrual cups and discs made from non-latex materials, designed for internal use during menstruation. These products are intended for single-user, long-term hygiene applications and are positioned as an alternative to disposable menstrual products.
The company’s products fall under FDA Class II regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. Nixit Limited operates from the United States, adhering to applicable U.S. medical device regulations.
Catalogue
- Registry: GUDID
Company details
- DUNS number
- 204591013
FDA establishments
- Nixit Limited Toronto Ontario · CA FEI 3014926189
Frequently asked questions
How many devices does Nixit Limited have in the registry?
The registry currently lists 1 device for Nixit Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nixit Limited's devices?
Among its 1 most recently registered device, Nixit Limited has devices listed in FDA GUDID (1 device).
What risk classes do Nixit Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nixit Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nixit Limited in the registry?
The most recently registered devices listed for Nixit Limited include nixit 00627987071368.
Which FDA establishments are linked to Nixit Limited?
1 FDA establishment is linked to Nixit Limited in the registry; they are listed on the company page.