# Ziip, LLC

> Medical device manufacturer record on deviCERTS, compiled from public registries. 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.

- Canonical page: <https://devicerts.com/manufacturers/ziip-llc>
- Also registered as: ZIIP INC
- Country: United States (FDA applicant, unverified)
- Role: Manufacturer

## Figures

- Devices: 11
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 9, FDA 510(k) 2
- Device classes: FDA Class II 11

## Devices

The first 11 of 11, in the order of the canonical page, which lists them all.

- [ZIIP Beauty LIPS](https://devicerts.com/devices/ziip-beauty-lips) · Class II · GUDID · status: Active
- [ZIIP Beauty EYES](https://devicerts.com/devices/ziip-beauty-eyes) · Class II · GUDID · status: Active
- [ZIIP Beauty HALO - CN](https://devicerts.com/devices/ziip-beauty-halo-cn) · Class II · GUDID · status: Active
- [ZIIP Beauty DOT - Grey](https://devicerts.com/devices/ziip-beauty-dot-grey) · Class II · GUDID · status: Active
- [ZIIP Beauty HALO](https://devicerts.com/devices/ziip-beauty-halo) · Class II · GUDID · status: Active
- [ZIIP Beauty DOT - Yellow](https://devicerts.com/devices/ziip-beauty-dot-yellow) · Class II · GUDID · status: Active
- [ZIIP Beauty Blush HALO](https://devicerts.com/devices/ziip-beauty-blush-halo) · Class II · GUDID · status: Active
- [ZIIP Beauty DOT - White](https://devicerts.com/devices/ziip-beauty-dot-white) · Class II · GUDID · status: Active
- [ZIIP Beauty DOT - Purple](https://devicerts.com/devices/ziip-beauty-dot-purple) · Class II · GUDID · status: Active
- [ZIIP+ Device](https://devicerts.com/devices/ziip-device-nfo-k212342) · ref K212342 · Class II · 510(k) · status: Active · decision 2021-09-23
- [ZIIP Device](https://devicerts.com/devices/ziip-device-nfo) · ref K161484 · Class II · 510(k) · status: Active · decision 2017-02-24

## Source and citation

- Cite as: Ziip, LLC. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/ziip-llc (data as of 2026-11-15).
- Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/ziip-llc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/ziip-llc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.