Establishment registration
ABBOTT VASCULAR
FDA establishment registration 2024168 · Temecula, US
Key facts
| Registration number | 2024168 |
|---|---|
| Establishment name | ABBOTT VASCULAR |
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| FEI number | 2024168 |
| Address | 26531 YNEZ RD. |
| City | Temecula |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DQK, DQO, DQX, DQY, DRG, DSA, DSK, DTL, DXO, DYB, DYG, FGE, FOX, IYO, KDQ, LDF, LIT, LOX, MAF, MAV, MGB, NIM, NIN, NIO, NIP, NIQ, NIV, NQQ, NTE, NXW and 2 more |
| Device classes | 1, 2, 3, f |
At a glance
- 100–999 Device listings
- 1,000+ 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