Establishment registration
Bausch & Lomb Incorporated
FDA establishment registration 1932180 · Manchester, US
Key facts
| Registration number | 1932180 |
|---|---|
| Establishment name | Bausch & Lomb Incorporated |
| Owner/operator | Bausch & Lomb Incorporated |
| Owner/operator number | 9913003 |
| FEI number | 1000119305 |
| Address | 499 SOVEREIGN CT. |
| City | Manchester |
| State | MO |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BWB, BYX, BYY, CAT, DWS, EID, EMF, EPY, EQJ, FFO, FGY, FHQ, FHR, FSM, FTY, FXE, FZO, FZS, FZX, GAB, GAC, GAD, GAZ, GBX, GDG, GDH, GDI, GDM, GDT, GDZ and 123 more |
| Device classes | 1, 2 |
At a glance
- 100–999 Device listings
- 100–999 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