Medical Device Manufacturer · US , East Lansing , MI

GreenMark Biomedical, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

GreenMark Biomedical, Inc. has 2 FDA 510(k) cleared medical devices. Based in East Lansing, US.

Latest FDA clearance: Jan 2025. Active since 2021. Primary specialty: Dental.

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

Regulatory submissions have been managed by Regulatory Technology Services, LLC and in2being, LLC.

FDA 510(k) Regulatory Record - GreenMark Biomedical, Inc.
2 devices
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