Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005724505

FEI Number

3005724505

Entity Name

ANECARE LLC

City/State/Country

SALT LAKE CITY, UT, US

Establishment Address

3333 West Parkway Blvd., SALT LAKE CITY, UT 84119, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

ANECARE LLC (Owner Number: 9086902)

Owner / Operator Contact Address

3333 West Parkway Blvd, --, Salt Lake City, UT 84119, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K033028

PMA Number

N/A

All Registered Proprietary Names

QED-100 ANEclear

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBN	Apparatus, Gas-Scavenging	Anesthesiology	Class 2	868.5430	2006-05-08
BYW	Device, Rebreathing	Anesthesiology	Class 1	868.5675	2006-05-08

Official Correspondent

Michael Slatter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANECARE 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 3005724505. Last updated year: 2026. Please use registration number 3005724505 when referencing this establishment in official correspondence.