MATERIALIZE BIO, INC.
Medtech · Private
Bioengineered ear tubes made from natural materials with on-demand removal capability
- Grants
- $1.5M
- 2 awards
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓2023202420252026
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | National Science Foundation · Phase I · SBIR Phase I: Bioengineered Next-Generation Tympanostomy Tubes to Improve Patient Outcomes | $274,999 | |
| Federal grant | National Science Foundation · Phase II · SBIR Phase II: Bioengineered Next-Generation Tympanostomy Tubes to Improve Patient Outcomes | $1,250,000 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1223 | EFEMORAL MEDICAL, INC. | — | $4.7M |
| 1224 | Happy Fireflies Ltd Liability Co | — | $2.0M |
| 1225 | VINE MEDICAL, INC. | — | $50K |
| 1226 | MATERIALIZE BIO, INC. | — | — |
| 1227 | Parallel Fluidics, Inc. | — | $5.2M |
| 1228 | CathAid Inc | — | $1.2M |
| 1229 | EPIC Imaging, P.C. | — | $222K |
Ranked on federal contract value rather than capital raised. The equity column is the comparison worth making — companies at the same procurement position often sit at very different points in their funding history.
Regulatory activity · Medtech
- New Animal Drugs; Approval of New Animal Drug Applications; Withdrawal of Approval of New Animal Drug Application; Change of SponsorFood and Drug Administration
- Medical Devices; General and Plastic Surgery Devices; Classification of the Skin Patch for Treatment of HyperhidrosisFood and Drug Administration
- Medical Devices; Anesthesiology Devices; Classification of the Monitor for Opioid Induced Impairment of OxygenationFood and Drug Administration
- Medical Devices; Orthopedic Devices; Classification of the Medial Knee Implanted Shock AbsorberFood and Drug Administration
- Medical Devices; Neurological Devices; Classification of the External Lower Extremity Nerve Stimulator for Restless Legs SyndromeFood and Drug Administration
- Medical Devices; General Hospital and Personal Use Devices; Classification of the Infant Supine Sleep SystemFood and Drug Administration
Rules are matched to sector, not to company. Recent activity in a sector is context rather than a signal about this business — until rules are matched to what a company actually builds, the section is shown as context and nothing more.