Daxwell, LLC is one of 16286 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, Powder Free Vinyl Patient Examination Gloves, Clear (non-colored)
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.
Regulatory submissions have been managed by Beijing Easylink Co., Ltd. and Beijing Believe-Med Technology Service Co., Ltd..
FDA 510(k) Regulatory Record - Daxwell, LLC
2 devices