Ziip, LLC
United StatesFDA applicant, unverified
Ziip, LLC is a medical device manufacturer, with 11 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 15 Nov 2026.
- Devices
- 11
Registry facts
- Registries
- FDA GUDID 9
- FDA 510(k) 2
- Device classes
- FDA Class II 11
What Ziip, LLC makes
Ziip, LLC manufactures facial muscle cosmesis electrical stimulators designed for non-invasive skin tightening and muscle activation. The devices are marketed under multiple iterations of the ZIIP Beauty brand and a standalone ZIIP Device model, targeting aesthetic improvements through electrical stimulation.
The company’s portfolio is regulated under FDA Class II devices, with authorisations recorded via 510(k) clearances and UDI listings. These devices are intended for use in the United States, where the manufacturer is based.
Catalogue
Search and filter all 11 devicesFrequently asked questions
How many devices does Ziip, Llc have in the registry?
The registry currently lists 11 devices for Ziip, Llc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ziip, Llc's devices?
Among its 11 most recently registered devices, Ziip, Llc has devices listed in FDA 510(k) (2 devices) and FDA GUDID (9 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Ziip, Llc's devices fall under?
Among its 11 most recently registered devices, the classes recorded for Ziip, Llc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ziip, Llc in the registry?
The most recently registered devices listed for Ziip, Llc include ZIIP Beauty LIPS, ZIIP Beauty EYES, ZIIP Beauty HALO - CN and ZIIP Beauty DOT - Grey.