Establishment registration
TECOMET, INC.
FDA establishment registration 2132732 · KENOSHA, US
Key facts
| Registration number | 2132732 |
|---|---|
| Establishment name | TECOMET, INC. |
| Owner/operator | Tecomet |
| Owner/operator number | 10031318 |
| FEI number | 1000306694 |
| Address | 5307 95th Ave |
| City | KENOSHA |
| State | WI |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EMH, FMH, FSM, FTY, FZO, FZT, FZX, GAD, GDF, GDI, GDJ, GDO, GDZ, GEA, GFA, GFC, GFI, GFJ, HAO, HBQ, HBT, HRH, HRT, HST, HTC, HTD, HTE, HTF, HTJ, HTO and 32 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 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