Category: Press Releases

GreenMark Biomedical Secures Follow-On Regenerative Medicine Grant Funding

August 25, 2026 Press Releases

ANN ARBOR, MI, UNITED STATES, August 25, 2026 – GreenMark Biomedical Inc. announces its project entitled “Targeted Remineralization Treatment Using Mineral Loaded Starch Nanoparticles” has been selected for additional funding by the Translational Resource Center. GreenMark will receive up to $297,615 in additional funding to advance new forms of its innovative regenerative products for noninvasive mineralization of early-stage […]

Read More

GreenMark Biomedical Secures Third NIH Grant in 2025

November 11, 2025 Press Releases

ANN ARBOR, MI, UNITED STATES, November 11, 2025 – GreenMark awarded NIH grant to advance its innovative regenerative technology for noninvasive mineralization of early-stage dental decay. GreenMark Biomedical Inc., a company developing innovative solutions for oral health, earlier this year was awarded funding via the Translational Resource Center (TRC) regenerative medicine program, as well as […]

Read More

Expanding GreenMark Biomedical Regenerative Dental Treatment Product Line

July 16, 2025 Press Releases

ANN ARBOR, MI, UNITED STATES, July 16, 2025 — GreenMark Biomedical Inc. announces its project entitled “Targeted Remineralization Treatment Using Mineral Loaded Starch Nanoparticles” has been selected for additional funding by the Translational Resource Center (TRC)’s Interdisciplinary Translational Project (ITP) program. GreenMark will receive up to $162,000 in additional funding to advance new forms of its innovative […]

Read More

GreenMark Secures FDA Clearance for CrystLCare™ PRO Biorestorative

January 7, 2025 Press Releases

ANN ARBOR, MI, UNITED STATES, January 7, 2025 – GreenMark Biomedical Inc., a pioneer in leveraging biomimetic technology for dental health innovations, today announced that the company has secured regulatory clearance from the U.S. Food and Drug Administration (FDA) to market its CrystLCare™ PRO Biorestorative, Fluoride-Plus product as a 510(k) Class II Medical Device.

Read More