Establishment registration
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.
FDA establishment registration 2085947 · CANOGA PARK, US
Key facts
| Registration number | 2085947 |
|---|---|
| Establishment name | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. |
| Owner/operator | NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. |
| Owner/operator number | 9027397 |
| FEI number | 3000204191 |
| Address | 22134 SHERMAN WAY |
| City | CANOGA PARK |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CCW, EOB, EPY, EQH, EQL, ERA, EZO, FAJ, FAS, FCW, FDC, FEM, FFR, FHQ, FJL, FSM, FSR, FWD, FWF, GAD, GCJ, GDO, GEI, GEN, GEY, HAE, HCF, HIH, HRX, HXD and 16 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 1–9 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