Medical Device Manufacturer · US , Chicago , IL

Visibly, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Total

Cleared

Denied

Visibly, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.

Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Visibly, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.

FDA 510(k) Regulatory Record - Visibly, Inc.

1 devices

1-1 of 1

Cleared CT Aug 12, 2022

Visibly Digital Acuity Product

K220090 · QTO

Ophthalmic · 213d

Regulatory Intelligence

Linked clinical trials FDA-regulated device evidence

Regulatory consultant 510(k) submission support ecosystem

Hogan Lovells US LLP

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 21, 2026

Visibly, Inc. - FDA 510(k) Cleared Devices

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