Conair Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conair Corporation - FDA 510(k) Cleared Devices
Recent clearances: Lumilisse IPL Hair Remover
1
Total
1
Cleared
0
Denied
Conair Corporation, is a consumer products company specializing in haircare, beauty, wellness, home, and travel solutions. The company operates with a manufacturing facility in Stamford, US.
Conair has received 1 FDA 510(k) clearance from 1 total submission in the General & Plastic Surgery category. The company's regulatory activity dates to 2018. As no clearances have been granted in more than five years, this record represents historical FDA regulatory engagement.
The company's cleared device portfolio includes aesthetic and cosmetic treatment technologies. Explore the device names, product codes, and clearance dates in the database for complete regulatory details.
510(k) submissions have been managed by Smith Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Conair Corporation
1 devices