Eye Academy of America Ltd.
DENVER, CO · CIK 0001679090 · Medtech
Custom-engineered contact lenses designed using advanced software
eye.space →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $4.0M
- 1 Form D · Jul 2016
- 123 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓2016
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $4,000,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1086 | DropletPharm Inc. | — | — |
| 1087 | EMANATE WIRELESS, INC. | — | $1.0M |
| 1088 | PSYONIC, Inc. | — | $150K |
| 1089 | Eye Academy of America Ltd. | — | $4.0M |
| 1090 | smallTalk Technology, Inc. | — | $1.1M |
| 1091 | Bansen Labs LLC | — | $300K |
| 1092 | UE LifeSciences Inc. | — | $480K |
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
- Brad AndersonDirector · Executive Officer
- Kris AndersonExecutive Officer
- Richard AndersonDirector · Executive Officer
- S. Ryan HeckmanDirector · Executive Officer
- Catherine O'DorisioDirector · Executive Officer
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.