THE AIRD
Medtech · Private
Adaptive Optics Optical Coherence Tomography (AO-OCT) system for high-resolution retinal imaging in small animal models
- Grants
- $305K
- 1 award
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- $120K
- 1 award · Veterans Affairs
- #506 of 4531 in medtech
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓202420252026
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal contract | Department of Veterans Affairs · Eyemera Oct | $120,000 | |
| Federal grant | Department of Health and Human Services · Phase I · Commercialization of Optical Coherence Tomography with Advanced Optical Design and Adaptive Optics for Rodent Eye | $305,000 |
Federal grant · SBIR/STTRFederal contract · USAspending
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 503 | HHITT, Inc. | $125K | $275K |
| 504 | FREYJA HEALTHCARE, LLC | $125K | — |
| 505 | AXCEND LLC | $123K | $7.2M |
| 506 | THE AIRD | $120K | — |
| 507 | SEATOX RESEARCH INC | $120K | — |
| 508 | SANUWAVE Health, Inc. | $117K | $81M |
| 509 | PURIGEN BIOSYSTEMS, INC. | $116K | $48M |
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.