Dimesol USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dimesol USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: Citric Complete Dry Citric Acid (45X)
1
Total
1
Cleared
0
Denied
Dimesol USA, LLC has 1 FDA 510(k) cleared medical devices. Based in Lewisberry, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dimesol USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcnees Wallace & Nurick, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dimesol USA, LLC
1 devices