Daxwell, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Daxwell, LLC - FDA 510(k) Cleared Devices
Recent clearances: Powder Free Nitrile Examination Glove
2
Total
2
Cleared
0
Denied
Daxwell, LLC has 2 FDA 510(k) cleared medical devices. Based in Houston, US.
Last cleared in 2022. Active since 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Daxwell, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beijing Believe-Med Technology Service Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Daxwell, LLC
2 devices