# Clarix Imaging > Medical device manufacturer record on deviCERTS, compiled from public registries. Clarix Imaging is a medical device manufacturer, with 2 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) as of 15 Nov 2026. - Canonical page: - Also registered as: CLARIX IMAGING CORP - Country: not established - Role: Manufacturer ## Figures - Devices: 2 - 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 510(k) 1, FDA GUDID 1 - Device classes: FDA Class II 2 ## Devices The first 2 of 2, in the order of the canonical page, which lists them all. - [Clarix Imaging Corps VSI-1](https://devicerts.com/devices/clarix-imaging-corps-vsi-1) · Class II · GUDID · status: Listed - [Volumetric Specimen Imager](https://devicerts.com/devices/volumetric-specimen-imager-mwp) · ref K192939 · Class II · 510(k) · status: Active · decision 2019-12-27 ## Source and citation - Cite as: Clarix Imaging. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/clarix-imaging (data as of 2026-11-15). - Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA GUDID](https://accessgudid.nlm.nih.gov/) - FDA recall data as of: 2026-11-01 - Data as of: 2026-11-15 - 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/clarix-imaging - 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.