MIDI, INC.
Biotech · Acquired
Automated analytical platform using HPLC, UHPLC, and GC with pattern recognition software to identify botanical components, detect adulteration, and quantify bioactive compounds in dietary supplements
- 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 ↓20182019
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal grant | Department of Health and Human Services · Phase I · Authentication quantitation and detection of adulteration in botanical dietary supplements using an automated chemometric platform | $148,641 |
Federal grant · SBIR/STTR
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1641 | LIGANDOMICSRX, LLC | — | — |
| 1642 | DOPHEN BIOMED, INC. | — | — |
| 1643 | T3S Technologies, Inc. | — | — |
| 1644 | MIDI, INC. | — | — |
| 1645 | CANCER TARGETED TECHNOLOGY, LLC | — | — |
| 1646 | IMMUNARTES LLC | — | — |
| 1647 | GENERAL NUTRACEUTICAL TECHNOLOGY 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.
Regulatory activity · Biotech
- 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.