Establishment registration
GULDEN OPHTHALMICS
FDA establishment registration 2518410 · Elkins Park, US
Key facts
| Registration number | 2518410 |
|---|---|
| Establishment name | GULDEN OPHTHALMICS |
| Owner/operator | GULDEN OPHTHALMICS INC |
| Owner/operator number | 2518410 |
| FEI number | 2518410 |
| Address | 225 CADWALADER AVE. |
| City | Elkins Park |
| State | PA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | FTY, HIT, HJF, HKD, HKQ, HKR, HKW, HLC, HLE, HLH, HLO, HLP, HLS, HMH, HMM, HNA, HNI, HNM, HOL, HON, HOQ, HOR, HOW, HOX, HOY, HPA, HPB, HPL, HPZ, HQN and 5 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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