Dimesol, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dimesol, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dimesol Disposable AV Fistula Needle Set (Non-Safety Series) and Dimesol Disposable AV Fistula Needle Set (Safety Series), Dimesol Tubing Sets for Hemodialysis
2
Total
2
Cleared
0
Denied
Dimesol, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lewisberry, US.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Dimesol, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Frost Brown Todd, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dimesol, Inc.
2 devices