Medical Device Manufacturer · US , Wood Dale , IL

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

8 submissions · 8 cleared · Since 1987

Recent clearances: C-QUEST, T-QUEST SYSTEM, MEDX NUQUEST - INTECAM SPECT 37-75 SYSTEM

View 8 510(k) Devices ↓

Total

Cleared

Denied

Medx, Inc. has 8 FDA 510(k) cleared medical devices. Based in Wood Dale, US.

Historical record: 8 cleared submissions from 1987 to 2008. Primary specialty: Radiology.

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

510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.

Medx, Inc. is one of 21396 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

8 devices

1-8 of 8

MEDX NUQUEST - INTECAM SPECT 37-75 SYSTEM

MEDX INTECAM INTERFACE

D-SCOPE II AND D-SCOPE IIC

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 11, 2026

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

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

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