Fresenius Medical Care Winter Lake, LLC
WALTHAM, MA · Founded 2021 · CIK 0001946107 · Medtech · Public
Dialysis devices and renal replacement therapy systems for kidney disease treatment
fresenius.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $3.6M
- 1 Form D · Sep 2022
- 49 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20222023
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $3,562,327 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 805 | NANOCAN THERAPEUTICS CORPORATION | — | $6.2M |
| 806 | XCath, Inc. | — | $5.3M |
| 807 | Prenosis, Inc. | — | $1.6M |
| 808 | Fresenius Medical Care Winter Lake, LLC | — | $3.6M |
| 809 | SISCAPA Assay Technologies, Inc. | — | $3.6M |
| 810 | Kerecis hf | — | $3.5M |
| 811 | Unify Medical Inc. | — | $2.8M |
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
- Ginine BrentarDirector
- Lisa EbertDirector
- Bao Huynh, M.D.Director
- Carrie LandDirector
- Mohammed Malas, M.D.Director
- Ryan ValleDirector
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.