Rua Diagnostics Inc.
WESTBURY, NY · Founded 2023 · CIK 0002133804 · Medtech · Private
Breath analysis diagnostic device using gas chromatography to detect volatile organic compounds for disease diagnosis
ruadiagnostics.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $3.6M
- 1 Form D · May 2026
- 5 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20252026
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $3,650,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2182 | LEEFA BIOTECH, LLC | — | — |
| 2183 | CALLAHAN-YOUNG LLC | — | — |
| 2184 | V-FLOW MEDICAL, INC. | — | — |
| 2185 | Rua Diagnostics Inc. | — | $3.6M |
| 2186 | TOI LABS, INC. | — | — |
| 2187 | BIONEX PHARMACEUTICALS, LLC | — | — |
| 2188 | C. LIGHT TECHNOLOGIES, 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.
Founders & Team
- David GooneDirector
- Jillian LevovitzExecutive Officer
- Peter MichalosDirector
- Jonathan OrrDirector · Executive Officer
- Kenneth OrrDirector
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.