METFORA LLC
Medtech · Private
Mass spectrometry-based diagnostic platform using circulating metabolite panels to detect pulmonary arterial hypertension
- Grants
- $629K
- 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 ↓202120222023
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · Profiling circulating metabolites for the diagnosis of pulmonary hypertension | $373,684 | |
| Federal grant | National Science Foundation · Phase I · SBIR Phase I: Detection of Chronic Diseases via Multiplex Analysis of Circulating Metabolites | $255,706 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 937 | Active Recovery TMS, LLC | — | $1.0M |
| 938 | OPTIVA FERTILITY, INC. | — | $3.0M |
| 939 | Prior Knowledge, Inc. | — | $2.0M |
| 940 | METFORA LLC | — | — |
| 941 | PeriCor LLC | — | — |
| 942 | Imbio, LLC | — | $1.1M |
| 943 | VISTA ENGINEERING, 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.