Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007137304

FEI Number

3007137304

Entity Name

COLLIMARE, LLC

City/State/Country

Golden, CO, US

Establishment Address

13401 W 43rd Dr Ste 7, Golden, CO 80403, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Collimare, LLC (Owner Number: 10026088)

Owner / Operator Contact Address

13401 W 43RD DR, STE 7, Golden, CO 80403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K073124

PMA Number

N/A

All Registered Proprietary Names

Collimare

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IZX	Collimator, Manual, Radiographic	Radiology	Class 2	892.1610	2008-06-06
IZW	Collimator, Automatic, Radiographic	Radiology	Class 2	892.1610	2008-06-06

Official Correspondent

Howard Thomas

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Collimare, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007137304. Last updated year: 2026. Please use registration number 3007137304 when referencing this establishment in official correspondence.