Establishment registration
CLEVELAND DIAGNOSTICS, INC.
FDA establishment registration 3011015335 · Cleveland, US
Key facts
| Registration number | 3011015335 |
|---|---|
| Establishment name | CLEVELAND DIAGNOSTICS, INC. |
| Owner/operator | Cleveland Diagnostics, Inc. |
| Owner/operator number | 10095401 |
| FEI number | 3011015335 |
| Address | 3615 Superior Ave Ste 4406a |
| City | Cleveland |
| State | OH |
| Country | US |
| Establishment types | Manufacturer, Repackager/relabeler, Single-use device reprocessor |
| Registration valid through | 2026 |
| Product codes listed | QRF |
| Device classes | 3 |
At a glance
- 1–9 Device listings
- 1–9 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