Carl Zeiss Jena GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carl Zeiss Jena GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Carl Zeiss Jena GmbH has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 2001 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Carl Zeiss Jena GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carl Zeiss Jena GmbH
1 devices