Establishment registration
LAUNCH DEVELOPMENT
FDA establishment registration 3011657089 · Dalton Gardens, US
Key facts
| Registration number | 3011657089 |
|---|---|
| Establishment name | LAUNCH DEVELOPMENT |
| Owner/operator | Launch Development |
| Owner/operator number | 10049473 |
| FEI number | 3011657089 |
| Address | 7791 Aqua Circle, Suite 7G |
| City | Dalton Gardens |
| State | ID |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | DRE, DYB, GEX |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database