Data / Medical devices / United States / Collimare, LLC
Collimare, LLC: FDA-registered device maker in Golden, CO, United States, 1 510(k) clearance
Collimare, LLC is registered with the FDA (registration 3007137304) in Golden, CO, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 16, 2007. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007137304
- Address
- 13401 W 43rd Dr Ste 7, Golden, CO, United States, 80403
- Owner or operator
- Collimare, LLC (10026088)
- Roles
- Manufacturer
- First device listed
- June 6, 2008
- Registered through
- 2026
- Brand names listed
- Collimare
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Collimator, Automatic, Radiographic | IZW | 2 | Manufacturer | accessdata.fda.gov |
| Collimator, Manual, Radiographic | IZX | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 16, 2007 | K073124 | COLLIMARE COLLIMATOR FAMILY | IZW | Substantially Equivalent | Collimare, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 16, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.