Medical Device Manufacturer · US , Denton , TX

Wide Corporation - FDA 510(k) Cleared Devices

20 submissions · 20 cleared · Since 2003

Recent clearances: CX50N, MX50N, CL24N

Total

Cleared

Denied

Wide Corporation has 20 FDA 510(k) cleared radiology devices. Based in Denton, US.

Last cleared in 2023. Active since 2003.

Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Ot Consulting, Inc. and Ot Consulting.

Wide Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Wide Corporation

20 devices

1-12 of 20

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026

Wide Corporation - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Wide Corporation

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