NANOPATHDX, INC.
Medtech · Private
Point-of-care molecular diagnostic assay cartridge with integrated nanosensor for rapid UTI pathogen and antibiotic resistance identification from urine
- Grants
- $2.0M
- 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 ↓202320242025
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase II · Multiplexed Assay for Point-of-Care UTI Diagnosis (ID/AMR) | $996,726 | |
| Federal grant | Department of Health and Human Services · Phase II · Multiplexed Assay for Point-of-Care UTI Diagnosis (ID/AMR) | $964,943 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1894 | Looking Glass Productions, LLC | — | $125K |
| 1895 | REQUISITE BIOMEDICAL, LLC | — | — |
| 1896 | POWERSCOPE, INC | — | — |
| 1897 | NANOPATHDX, INC. | — | — |
| 1898 | QATCH TECHNOLOGIES LLC | — | — |
| 1899 | VISO Therapeutics Inc. | — | — |
| 1900 | ORB XYZ, 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.