Establishment registration
ABBOTT LABORATORIES
FDA establishment registration 3005333358 · Lake Forest, US
Key facts
| Registration number | 3005333358 |
|---|---|
| Establishment name | ABBOTT LABORATORIES |
| Owner/operator | ABBOTT LABORATORIES |
| Owner/operator number | 1415939 |
| FEI number | 3005333358 |
| Address | Conway Park |
| City | Lake Forest |
| State | IL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDD, CDO, CDP, CDQ, CDT, CDZ, CEC, CEK, CEM, CEO, CEP, CEW, CFJ, CFP, CFR, CFT, CGJ, CGN, CGS, CGX, CGZ, CHH, CHI, CHP, CIG, CIT, CIX, CJE, CJW, CJY and 162 more |
| Device classes | 1, 2, 3, N, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- None 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