Sequence46, LLC
LOS ANGELES, CA · Founded 2017 · CIK 0001804148 · Biotech · Private
Preimplantation genetic testing (PGT) for IVF embryo screening
sequence46.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $48K
- 1 Form D · Feb 2020
- 79 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20192020
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $48,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 2673 | Advanced Gene Transfer Company, Inc. | — | — |
| 2674 | ITERION THERAPEUTICS INC. | — | — |
| 2675 | Qu Biologics Inc. | — | $49K |
| 2676 | Sequence46, LLC | — | $48K |
| 2677 | Forkhead Biotherapeutics, Inc. | — | — |
| 2678 | Arcus, Inc. | — | $35K |
| 2679 | Extended Longevity, Inc. | — | $10K |
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
- Susan ChristoffersonExecutive Officer
- Kyle FrancisExecutive Officer
- Gary NakhudaExecutive Officer
- Sophia TormasiPromoter
- Catherine WelchDirector · Executive Officer · Promoter
Regulatory activity · Biotech
- 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.