GreenMark Biomedical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
GreenMark Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CrystLCare™ PRO Biorestorative, Fluoride-Plus, LumiCare Caries Diagnostic Rinse
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 in2being, LLC and Regulatory Technology Services, LLC.
FDA 510(k) Regulatory Record - GreenMark Biomedical, Inc.
2 devices