# Collimare, LLC

> Medical device manufacturer record on deviCERTS, compiled from public registries. Collimare, LLC is a medical device manufacturer, with 8 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/collimare-llc>
- Country: United States (from the FDA registration address)
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 3007137304
- DUNS: 626743954

## Figures

- Devices: 8
- 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 7, FDA 510(k) 1
- Device classes: FDA Class II 8

## Devices

The first 8 of 8, in the order of the canonical page, which lists them all.

- [Collimare CPL-125-MX01-C](https://devicerts.com/devices/collimare-cpl-125-mx01-c) · Class II · GUDID · status: Active
- [Collimare CML-125-0001-C](https://devicerts.com/devices/collimare-cml-125-0001-c) · Class II · GUDID · status: Active
- [Collimare CTL-150-0001-C](https://devicerts.com/devices/collimare-ctl-150-0001-c) · Class II · GUDID · status: Active
- [Collimare CML-150-0001-C](https://devicerts.com/devices/collimare-cml-150-0001-c) · Class II · GUDID · status: Active
- [Collimare CPL-125-SR01-C](https://devicerts.com/devices/collimare-cpl-125-sr01-c) · Class II · GUDID · status: Active
- [Collimare CML-150-CMR1-C](https://devicerts.com/devices/collimare-cml-150-cmr1-c) · Class II · GUDID · status: Active
- [Collimare CPL-125-0001-C](https://devicerts.com/devices/collimare-cpl-125-0001-c) · Class II · GUDID · status: Active
- [Collimare Collimator Family](https://devicerts.com/devices/collimare-collimator-family-izw) · ref K073124 · Class II · 510(k) · status: Active · decision 2007-11-16

## Source and citation

- Cite as: Collimare, LLC. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/collimare-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 registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/collimare-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/collimare-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.