Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021241872

FEI Number

3021241872

Entity Name

C-CLEAR LLC

City/State/Country

Salt Lake City, UT, US

Establishment Address

6804 South 1300 East, Salt Lake City, UT 84121, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

C-Clear LLC (Owner Number: 10083628)

Owner / Operator Contact Address

6804 South 1300 East, Salt Lake City, UT 84121, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

C-Clear Baton

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2021-12-16

Official Correspondent

Wayne Shortt

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

C-Clear 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 3021241872. Last updated year: 2026. Please use registration number 3021241872 when referencing this establishment in official correspondence.