Establishment registration
ARMM, INC.
FDA establishment registration 2028523 · HUNTINGTON BEACH, US
Key facts
| Registration number | 2028523 |
|---|---|
| Establishment name | ARMM, INC. |
| Owner/operator | ARMM, INC. |
| Owner/operator number | 9005125 |
| FEI number | 1000125147 |
| Address | 17744 SAMPSON LN. |
| City | HUNTINGTON BEACH |
| State | CA |
| Country | US |
| Establishment types | Remanufacturer |
| Registration valid through | 2026 |
| Product codes listed | BTR, BYY, DRF, DTS, DWS, DZN, EMJ, EMR, FYD, GAZ, GBN, GBX, GCJ, GDF, GDW, GEI, GFF, HIF, HKP, HPZ, HQE, HQN, HRS, HWE, HWK, HXI, JOL, KDH, KGZ, KYG and 10 more |
| Device classes | 1, 2, 3 |
At a glance
- 10–99 Device listings
- 10–99 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