Medical Device Manufacturer · US , Redwood City , CA

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

1 submissions · 1 cleared · Since 2021

Total

Cleared

Denied

Carrot, Inc. has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.

Last cleared in 2021. Active since 2021. Primary specialty: Toxicology.

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

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

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

1 devices

1-1 of 1

Cleared CT Jun 30, 2021

Pivot Breath Sensor

K201206 · CCJ

Toxicology · 422d

Regulatory Intelligence

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Hogan Lovells US LLP

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 24, 2026

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

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