Establishment registration
AXIODENT INC.
FDA establishment registration 3032312561 · Wilmington, US
Key facts
| Registration number | 3032312561 |
|---|---|
| Establishment name | AXIODENT INC. |
| Owner/operator | Axiodent Inc. |
| Owner/operator number | 10091372 |
| FEI number | 3032312561 |
| Address | 501 Silverside Rd Ste 105 # 5086 |
| City | Wilmington |
| State | DE |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EBF, EBG, EEA, EGD, EJK, EJR, ELW, EMA, EMB, KIF, KLE, NDP |
| Device classes | 1, 2 |
At a glance
- 10–99 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