Sublime Laser, Inc.
Salt Lake City, UT · Founded 2022 · CIK 0001958691 · Medtech · Private
Laser-machined medical device components using femtosecond laser technology
sublimelaser.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $2.5M
- 3 Form D · Mar 2024
- 30 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓202220232024
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $2,210,000 | |
| Private capital raised | Form D · SEC | $280,000 | |
| Private capital raised | Form D · SEC | $50,000 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 1284 | AMIRA HEALTH INC. | — | $2.6M |
| 1285 | Matrix Industries, Inc. | — | $51M |
| 1286 | COPRATA, INC. | — | — |
| 1287 | Sublime Laser, Inc. | — | $2.5M |
| 1288 | PharmaPrinter LLC | — | — |
| 1289 | Vistim Labs Inc. | — | $405K |
| 1290 | 3DP Security Inc | — | — |
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
- Robert ChangDirector
- Jing LiDirector
- Todd TurnlundDirector · 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.