Establishment registration
LASKO PRODUCTS LLC
FDA establishment registration 1000190272 · West Chester, US
Key facts
| Registration number | 1000190272 |
|---|---|
| Establishment name | LASKO PRODUCTS LLC |
| Owner/operator | Lasko Products LLC |
| Owner/operator number | 10080646 |
| FEI number | 1000190272 |
| Address | 820 Lincoln avenue |
| City | West Chester |
| State | PA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | KFZ |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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