FLOWPOINT MEDICAL INC
Medtech · Private
Implantable vascular access device with 3D-printed titanium shell and titanium-nitride coated valve for hemodialysis needle guidance
- Grants
- $380K
- 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 ↓20242025
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · Self-sealing needle guide system for reliable hemodialysis | $324,836 | |
| Federal grant | Department of Health and Human Services · Phase I · Self-sealing needle guide system for reliable hemodialysis | $55,000 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1823 | RIO PHARMACEUTICALS, INC. | — | — |
| 1824 | iMacular Regeneration LLC | — | — |
| 1825 | Caris Life Sciences | — | — |
| 1826 | FLOWPOINT MEDICAL INC | — | — |
| 1827 | LF PRINTECH LLC | — | — |
| 1828 | APPLIED NANOSTRUCTURES, INC. | — | — |
| 1829 | Hawai'i Innovation Laboratory, Inc. | — | — |
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.