Establishment registration
Ortho-Clinical Diagnostics
FDA establishment registration 3007111389 · Pencoed Bridgend, GB
Key facts
| Registration number | 3007111389 |
|---|---|
| Establishment name | Ortho-Clinical Diagnostics |
| Owner/operator | QuidelOrtho Corporation |
| Owner/operator number | 2024674 |
| FEI number | 3007111389 |
| Address | Felindre Meadows |
| City | Pencoed Bridgend |
| Country | GB |
| Establishment types | Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | CDD, CDP, CDZ, CEC, CEP, CEW, CFT, CGJ, CGN, CGR, CHP, DBF, DDR, DHA, DHX, JHX, JIS, JIT, JIX, JJE, JJX, JJY, JKD, JLS, JLW, JMM, KHQ, KLI, LFX, LOJ and 20 more |
| Device classes | 1, 2, N |
At a glance
- 10–99 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