Edma Group, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Edma Group, LLC - FDA 510(k) Cleared Devices
Recent clearances: Edma Synthetic Nitrile Examination Gloves, Edma Nitrile Examination Gloves (Tested for Use with Chemotherapy Drugs)
2
Total
2
Cleared
0
Denied
Edma Group, LLC has 2 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Edma Group, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Truthful Information Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Edma Group, LLC
2 devices