Binder GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Binder GmbH - FDA 510(k) Cleared Devices
Recent clearances: BINDER CO2 INCUBATOR SERIE CB
1
Total
1
Cleared
0
Denied
Binder GmbH has 1 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Binder GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Binder GmbH
1 devices