Establishment registration
MOLTENO OPHTHALMIC LTD.
FDA establishment registration 3001227772 · DUNEDIN Otago, NZ
Key facts
| Registration number | 3001227772 |
|---|---|
| Establishment name | MOLTENO OPHTHALMIC LTD. |
| Owner/operator | MOLTENO OPHTHALMIC LTD. |
| Owner/operator number | 9030682 |
| FEI number | 3001227772 |
| Address | 152 FREDERICK ST. |
| City | DUNEDIN Otago |
| Country | NZ |
| Registration valid through | 2026 |
| Product codes listed | KYF |
| Device classes | 2 |
At a glance
- 1–9 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