Establishment registration
LUTHER NEEDLESAFE PRODUCTS LLC
FDA establishment registration 3017129766 · Laguna Hills, US
Key facts
| Registration number | 3017129766 |
|---|---|
| Establishment name | LUTHER NEEDLESAFE PRODUCTS LLC |
| Owner/operator | Luther Needlesafe Products LLC |
| Owner/operator number | 10087391 |
| FEI number | 3017129766 |
| Address | 26052 Merit Cir Ste 107 |
| City | Laguna Hills |
| State | CA |
| Country | US |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | FOZ |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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