Establishment registration
MINNETRONIX, INC.
FDA establishment registration 2133810 · Saint Paul, US
Key facts
| Registration number | 2133810 |
|---|---|
| Establishment name | MINNETRONIX, INC. |
| Owner/operator | Minnetronix Medical, Inc. |
| Owner/operator number | 9033484 |
| FEI number | 3000203066 |
| Address | 1635 ENERGY PARK DR. |
| City | Saint Paul |
| State | MN |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BZC, BZG, DQK, DSQ, DWJ, GCJ, GEI, GZT, HRX, ITX, IYN, IYO, KNT, KNW, KZA, KZL, LBI, LGW, MCX, MRN, OAE, OCL, OCM, OLO, PJZ, QBC, QCD, QEF, QHJ, QNR and 2 more |
| Device classes | 1, 2, 3 |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- 10–99 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