UNITED ORTHOPEDIC GROUP, INC.
PLANO, TX · CIK 0001438015 · Medtech · Acquired
Orthopedic implants for hip and knee replacement
unitedorthopedic.com →- Grants
- —
- No SBIR or STTR on record
- Sector median: 1
- Raised
- $2.1M
- 1 Form D · May 2013
- 160 months since last filing
- Contracts
- —
- No federal contracts on record
- Patents
- —
- No published records under this name
- Sector median: 2
Capital Timeline
Federal ↑Equity ↓20122013
| Date | Event | Source | Amount |
|---|---|---|---|
| Private capital raised | Form D · SEC | $2,105,265 |
Form D · SEC
Peer position
| # | Company | Contracts | Disclosed equity |
|---|---|---|---|
| 892 | STRATEGIC PACING SYSTEMS LLC | — | — |
| 893 | Cernostics Inc | — | $16M |
| 894 | Sanuwave, Inc. | — | $1.4M |
| 895 | UNITED ORTHOPEDIC GROUP, INC. | — | $2.1M |
| 896 | OPTIMOTION IMPLANTS LLC | — | $2.3M |
| 897 | Sutter Fairfield Surgery Center, LLC | — | $972K |
| 898 | X-SCAN IMAGING CORP | — | $600K |
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
- R. BarryDirector
- Gary BledsoeDirector
- Gary HenleyDirector · Executive Officer
- Gregory NelsonDirector
- Mark PacalaDirector
- Kimberly PinsonExecutive Officer
- William SchmidtDirector
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.