Establishment registration
PeriGen Solutions Ltd.
FDA establishment registration 9615396 · Rishon LeTziyon Central, IL
Key facts
| Registration number | 9615396 |
|---|---|
| Establishment name | PeriGen Solutions Ltd. |
| Owner/operator | PeriGen, Inc. |
| Owner/operator number | 10030146 |
| FEI number | 3002687025 |
| Address | Azriel Rishonim, 10th Floor, Sderot Nim2 |
| City | Rishon LeTziyon Central |
| Country | IL |
| Registration valid through | 2026 |
| Product codes listed | HGM |
| 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