Medical Device Manufacturer · US , Harrytown , NY

Oreon Technologies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2016

Total

Cleared

Denied

Oreon Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Harrytown, US.

Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Oreon Technologies, Inc.

1 devices

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