Braun AG is one of 9755 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Braun AG - FDA 510(k) Cleared Devices
Recent clearances: BRAUN THERMOSCAN IRT3020/3500 ONE SECONS EAR THERMOMETER, MODEL IRT3020/3520
1
Total
1
Cleared
0
Denied
Braun AG, is a global personal care company specializing in electric shavers, grooming tools, and epilation devices. The company operates with a manufacturing facility in San Diego, US, and is part of the Procter & Gamble portfolio.
Braun has received 1 FDA 510(k) clearance from 1 total submission in the General Hospital device category. The company's regulatory activity dates to 1999, when it cleared the BRAUN THERMOSCAN IRT3020/3500 One Second Ear Thermometer. No new clearances have been submitted in over two decades, making this a historical regulatory record.
Explore the device names, product codes, and clearance dates in the database to learn more about Braun's FDA 510(k) history.
FDA 510(k) Regulatory Record - Braun AG
1 devices