NCAP MEDICAL, LLC
Medtech · Private
NEUROCUPLE, a nonpharmacological neuromodulation device for postoperative pain relief after knee replacement surgery
- Grants
- $416K
- 1 award
- Sector median: 1
- Raised
- —
- No Form D on record
- Contracts
- $111K
- 1 award · Homeland Security
- #512 of 4531 in medtech
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓202220232024
| Date | Event | Source | Amount |
|---|---|---|---|
| Federal contract | Department of Homeland Security · Provide Fema Region 10 With A G-197 Curriculum Development Course | $111,359 | |
| Federal grant | Department of Health and Human Services · Phase I · Enhancing pain management for knee replacement patients through an innovative non-invasive and opioid-sparing device | $416,443 |
Federal grant · SBIR/STTRFederal contract · USAspending
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 509 | PURIGEN BIOSYSTEMS, INC. | $116K | $48M |
| 510 | Egg Medical, Inc. | $115K | $28M |
| 511 | CDI LABORATORIES, INC | $112K | $3.3M |
| 512 | NCAP MEDICAL, LLC | $111K | — |
| 513 | GREAT LAKES NEUROTECHNOLOGIES INC. | $109K | — |
| 514 | ALM Ortho Inc | $107K | $135K |
| 515 | INFINITE BIOMEDICAL TECHNOLOGIES, LLC | $105K | — |
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.