Establishment registration
RESCUE SHOT CASE
FDA establishment registration 3016937081 · Long Branch, US
Key facts
| Registration number | 3016937081 |
|---|---|
| Establishment name | RESCUE SHOT CASE |
| Owner/operator | rescue Shot Case |
| Owner/operator number | 10093932 |
| FEI number | 3016937081 |
| Address | 735 Hoey Ave |
| City | Long Branch |
| State | NJ |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | KGB, KPY |
| 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