Visant Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Visant Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Visant Medical Canalicular Plug
1
Total
1
Cleared
0
Denied
Visant Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Visant Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Pathways Group, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Visant Medical, Inc.
1 devices