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SUNSET HEALTHCARE SOLUTIONS, Inc.

Also registered as Sunset Healthcare Solutions, LLC

United Statesfrom the FDA registration address FDA establishment FEI 3006446479

SUNSET HEALTHCARE SOLUTIONS, Inc. is a medical device manufacturer, with 1 device listed in FDA 510(k) (FDA Class II) as of 12 Nov 2026.

Devices
1
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA 510(k) 1
Device classes
  • FDA Class II 1
Identifiers
  • FDA FEI 3006446479

What SUNSET HEALTHCARE SOLUTIONS, Inc. makes

Sunset Healthcare Solutions, Inc. manufactures reusable and single-use respiratory filters for CPAP/BPAP units, including ambient air filters and anesthesia conduction filters, as well as reusable and single-use inspiratory/expiratory limb respiratory tubing. The company also produces CPAP/BPAP face masks, oxygen administration kits, closed-suction breathing circuit connectors, and tracheostomy ties. Additional products include circuit connectors, convenience kits, and specialized filters for anesthesia and ventilator use.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3006446479
Address
141 W Jackson Blvd Ste 1950, CHICAGO, IL, 60604

Frequently asked questions

How many devices does SUNSET HEALTHCARE SOLUTIONS, Inc. have in the registry?

The registry currently lists 1 device for SUNSET HEALTHCARE SOLUTIONS, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list SUNSET HEALTHCARE SOLUTIONS, Inc.'s devices?

Among its 1 most recently registered device, SUNSET HEALTHCARE SOLUTIONS, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do SUNSET HEALTHCARE SOLUTIONS, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for SUNSET HEALTHCARE SOLUTIONS, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from SUNSET HEALTHCARE SOLUTIONS, Inc. in the registry?

The most recently registered devices listed for SUNSET HEALTHCARE SOLUTIONS, Inc. include SUNSET HEALTHCARE SOLUTIONS BACTERIAL/VIRAL HME FILTER, MODEL BHF 104.

Generated automatically from registry data and not verified by a human reviewer.

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.