Circulate Health, Inc.
SEATTLE, WA · Founded 2021 · CIK 0002078196 · Medtech · Acquired
circulate.health →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $11M
- 1 Form D · Oct 2025
- 12 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓202520262027
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $10,600,001 |
Form D · SECPress
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1492 | Byonyks Medical Devices, Inc. | — | $1.0M |
| 1493 | Telesair, Inc. | — | $26M |
| 1494 | WASATCH PHOTONICS, INC. | — | — |
| 1495 | Circulate Health, Inc. | — | $11M |
| 1496 | IRONSIDES MEDICAL INC | — | — |
| 1497 | NeuroQore, Inc. | — | $1.5M |
| 1498 | VIROLOCK TECHNOLOGIES LIMITED LIABILITY COMPANY | — | — |
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.
Press
Viome Acquires Circulate Health To Combine Precision Diagnostics With Therapeutic Plasma ExchangePulse 2.0
Founders & Team
- Uri GreenwaldDirector
- Robbie SchwietzerExecutive Officer
- Brad YounggrenDirector · Executive Officer · Promoter
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.