Medical Device Manufacturer · US , Littleton , CO

Caire, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1995

Total

Cleared

Denied

Caire, Inc. has 7 FDA 510(k) cleared medical devices. Based in Littleton, US.

Latest FDA clearance: Jul 2025. Active since 1995. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Caire, Inc. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Tuv Product Service, Inc. and Intertek Testing Services.

Caire, Inc. is one of 16067 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Caire, Inc.

7 devices

1-7 of 7

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Apr 27, 2026