Establishment registration
CHARMANT U.S.A.
FDA establishment registration 2248180 · Morris Plains, US
Key facts
| Registration number | 2248180 |
|---|---|
| Establishment name | CHARMANT U.S.A. |
| Owner/operator | CHARMANT, INC. |
| Owner/operator number | 9001784 |
| FEI number | 1000307813 |
| Address | 400 AMERICAN RD. |
| City | Morris Plains |
| State | NJ |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DWS, EMF, FYF, GDI, GDL, GDO, GZX, HBM, HMX, HNC, HND, HNF, HNH, HNM, HNN, HNQ, HNR, HOE, HOH, HOI, HQY, HQZ, HXD, JOL, JZF, KAE, KAL, KAO, KTG, LRW and 2 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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