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Collimare, LLC

United Statesfrom the FDA registration address FDA FEI 3007137304

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.

Devices
8
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 15 Nov 2026

Registries
  • FDA GUDID 7
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 8
Identifiers
  • FDA FEI 3007137304
  • DUNS 626743954

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Collimare, LLC makes

Collimare, LLC makes manual-aperture-control diagnostic x-ray system collimators.

Its devices are listed in the FDA 510(k) premarket notification database and the FDA GUDID device identification database. The listed devices are recorded as Class II.

AI-generated from registry data, 27 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

  • Collimare CPL-125-MX01-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CML-125-0001-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CTL-150-0001-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CML-150-0001-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CPL-125-SR01-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CML-150-CMR1-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare CPL-125-0001-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Collimare Collimator Family Ref K073124

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

FDA FEI number
3007137304
DUNS number
626743954
Address
13401 W 43rd Dr Ste 7, Golden, CO, 80403
Phone
3038097184

Frequently asked questions

How many devices does Collimare, LLC have in the registry?

The registry currently lists 8 devices for Collimare, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Collimare, LLC's devices?

Among its 8 most recently registered devices, Collimare, LLC has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Collimare, LLC's devices fall under?

Among its 8 most recently registered devices, the classes recorded for Collimare, LLC's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Collimare, LLC in the registry?

The most recently registered devices listed for Collimare, LLC include Collimare CPL-125-MX01-C, Collimare CML-125-0001-C, Collimare CTL-150-0001-C and Collimare CML-150-0001-C.

Generated automatically from registry data and not verified by a human reviewer.