BIOGRAFT, INC.
Stanford, CA · Medtech · Private
External biodegradable scaffold device to prevent saphenous vein graft failure after coronary artery bypass surgery
- Grants
- $345K
- 1 award
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- —
- No federal contracts on record
- Patents
- 1
- 0 granted · 1 pending
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20222023
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · Preclinical testing of a 3D printed external scaffold device to prevent vein graft failure after coronary bypass graft surgery | $345,103 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 678 | LumiraDx Ltd | — | $682M |
| 679 | ADVANCED VASCULAR THERAPIES, INC. | — | — |
| 680 | STARK STREET MATERIALS COMPANY | — | — |
| 681 | BIOGRAFT, INC. | — | — |
| 682 | ZIMMER BIOMET HOLDINGS, INC. | — | $216M |
| 683 | NUMENTUS TECHNOLOGIES INC | — | — |
| 684 | ECATE LLC | — | — |
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.
Patents
- Vascular Graft Assemblies, Vascular Graft Systems, And Methods Of Use Thereofapplication
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.