Medical Device Manufacturer · US , Golden Valley , MN

Green Or, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Green Or, LLC has 1 FDA 510(k) cleared medical devices. Based in Golden Valley, US.

Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.

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

510(k) submissions have been managed by Pathway, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Green Or, LLC

1 devices
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