AUGDIMER, LLC
Medtech
Provoked D-Dimer (PDD) assay—an improved blood test for venous thromboembolism that adds thrombolytics in vitro to enhance specificity and positive predictive value over standard D-Dimer testing
- Grants
- $149K
- 1 award
- 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 ↓20192020
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · The Diagnostic Utility of the in-vitro "Provoked" D dimer test in patients with suspected pulmonary embolism | $148,864 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1002 | Lumafield | — | — |
| 1003 | Cam2Technologies, LLC | — | — |
| 1004 | DrinkSavvy, Inc. | — | — |
| 1005 | AUGDIMER, LLC | — | — |
| 1006 | LifeAire Systems, LLC | — | $2.3M |
| 1007 | NVIZIX LLC | — | — |
| 1008 | Nervana Systems, Inc. | — | $24M |
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.