Establishment registration
CULVER TOOL & ENGINEERING
FDA establishment registration 3010047454 · Plymouth, US
Key facts
| Registration number | 3010047454 |
|---|---|
| Establishment name | CULVER TOOL & ENGINEERING |
| Owner/operator | Culver Tool & Engineering LLC dba SpiTrex CTE |
| Owner/operator number | 10043008 |
| FEI number | 3010047454 |
| Address | 1901 Walter Glaub Dr |
| City | Plymouth |
| State | IN |
| Country | US |
| Establishment types | Manufacturer, Contract sterilizer |
| Registration valid through | 2026 |
| Product codes listed | ETN, FLL, FSM, FZX, FZY, GAD, GAT, GWF, GXN, HAW, HRS, HSB, HTN, HTO, HTR, HTW, HTX, HWC, HWD, HWE, HWJ, HWP, HWQ, HWT, HWX, HXB, HXC, HXG, HXX, IKN and 36 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 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