# Kinsa, Inc.

- Location (FDA's records): San Francisco, CA
- FDA decisions: 2 (2013–2018): 2 510(k) clearances
- Product codes: FLL (2)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Fudakang Industries Co., Ltd.: 1 (https://510kreport.com/company/fudakang-industries)

## Firms that cite its devices most
- Famidoc Technology Co., Ltd.: 1 (https://510kreport.com/company/famidoc-technology)
- Xiamen Intretech, Inc.: 1 (https://510kreport.com/company/xiamen-intretech)
- Guangdong Biolight Meditech Co., Ltd.: 1 (https://510kreport.com/company/guangdong-biolight-meditech)

## Its most-cited devices
- K173730: Kinsa QuickCare Thermometer (2018), cited by 2
- K132514: Kinsa Smart Thermometer (2013), cited by 1

## Recent decisions
- K173730: Kinsa QuickCare Thermometer (Jan 17, 2018)
- K132514: Kinsa Smart Thermometer (Dec 2, 2013)

Source page: https://510kreport.com/company/kinsa