Establishment registration
INSTRUMENTATION LABORATORY CO.
FDA establishment registration 2431530 · ORANGEBURG, US
Key facts
| Registration number | 2431530 |
|---|---|
| Establishment name | INSTRUMENTATION LABORATORY CO. |
| Owner/operator | Instrumentation Laboratory Co. |
| Owner/operator number | 1217183 |
| FEI number | 2431530 |
| Address | 526 Route 303 |
| City | ORANGEBURG |
| State | NY |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | CDQ, CEM, CGA, CGZ, CHL, CIG, DLJ, GFO, GGC, GGN, GGP, GGW, GHS, GIR, GIS, GIZ, GJA, GJS, GJT, GKF, GKR, GLK, GLY, JBQ, JFO, JFP, JFY, JGS, JIS, JIT and 14 more |
| Device classes | 1, 2, N |
At a glance
- 10–99 Device listings
- 1,000+ 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