Medical Device Manufacturer · US , Menlo Park , CA

Visant Medical, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

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

1-1 of 1

Cleared CT Dec 23, 2022

Visant Medical Canalicular Plug

K222164 · LZU

Ophthalmic · 155d

Regulatory Intelligence

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Regulatory Pathways Group, Inc.

Regulatory activity signals

510(k) clearance pathway relevance detected

Medical device regulatory intelligence node

Consulting ecosystem involvement present

Clinical validation data available

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 20, 2026

Visant Medical, Inc. - FDA 510(k) Cleared Devices

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