Establishment registration
RMS CO.
FDA establishment registration 2183946 · MINNEAPOLIS, US
Key facts
| Registration number | 2183946 |
|---|---|
| Establishment name | RMS CO. |
| Owner/operator | THE CRETEX COMPANIES, INC. |
| Owner/operator number | 9001389 |
| FEI number | 1000116116 |
| Address | 8600 EVERGREEN BLVD. |
| City | MINNEAPOLIS |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DZK, ETN, GFC, GWF, GXZ, GZT, HRS, HSB, HSD, HTN, HTY, HWC, HWD, IKN, JDB, JDK, JDQ, JDR, JDW, JWH, JWJ, KRO, KTT, KWD, KWG, KWI, KWP, KWQ, KWS, KWT and 29 more |
| Device classes | 1, 2, 3, f, N, U |
At a glance
- 100–999 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