Establishment registration
PRO-TECH DESIGN & MFG., INC.
FDA establishment registration 2032521 · SANTA FE SPRINGS, US
Key facts
| Registration number | 2032521 |
|---|---|
| Establishment name | PRO-TECH DESIGN & MFG., INC. |
| Owner/operator | PRO-TECH Design & Mfg, Inc. |
| Owner/operator number | 9048910 |
| FEI number | 3003574398 |
| Address | 14561 MARQUARDT AVE. |
| City | SANTA FE SPRINGS |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | BSP, BTQ, DRB, DRE, DTB, DXY, FMF, FPA, GCJ, GCQ, GXI, GXR, GZB, GZF, HET, HNN, HRX, HSD, HTN, HWC, IQG, JKA, JQC, JWH, JWJ, KRG, KTT, KWD, KWP, KWS and 32 more |
| Device classes | 1, 2, 3, U |
At a glance
- 10–99 Device listings
- None 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