Pixie Cup, LLC
Country not established
Pixie Cup, LLC is a medical device manufacturer, with 49 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 15 Nov 2026.
- Devices
- 49
Registry facts
- Registries
- FDA GUDID 48
- FDA 510(k) 1
- Device classes
- FDA Class II 42
- FDA Class I 7
- Identifiers
- DUNS 028513002
What Pixie Cup, LLC makes
Pixie Cup, LLC manufactures reusable menstrual cups and discs made without latex, electric heating pads designed for localized body warmth, and steam sterilizers for cleaning reusable medical devices. The company also produces reusable vaginal applicators. These products are intended for personal hygiene and medical device sterilization.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with some products listed via 510(k) and UDI registrations. The manufacturer operates in the United States.
Catalogue
Search and filter all 49 devicesCompany details
- DUNS number
- 028513002
- info@pixiecup.com
- Phone
- 4172430677
Frequently asked questions
How many devices does Pixie Cup, LLC have in the registry?
The registry currently lists 49 devices for Pixie Cup, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pixie Cup, LLC's devices?
Among its 49 most recently registered devices, Pixie Cup, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (48 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Pixie Cup, LLC's devices fall under?
Among its 49 most recently registered devices, the classes recorded for Pixie Cup, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pixie Cup, LLC in the registry?
The most recently registered devices listed for Pixie Cup, LLC include Pixie Cup B09NQDYZMW, Pixie Cup B0BFNLQC4L, Pixie Cup B0GMXXDH8J and Pixie Cup B0GMT9C1KH.