Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017726824

FEI Number

3017726824

Entity Name

Tensentric, LLC

City/State/Country

Louisville, CO, US

Establishment Address

474 South Taylor Ave, Suite C, Louisville, CO 80027, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Tensentric (Owner Number: 10079361)

Owner / Operator Contact Address

2900 Center Green Court, Boulder, CO 80301, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Carepath

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EXY	Uroflowmeter	Gastroenterology, Urology	Class 2	876.1800	2020-12-07

Official Correspondent

Michelle Pratte

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tensentric

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 3017726824. Last updated year: 2026. Please use registration number 3017726824 when referencing this establishment in official correspondence.