Establishment registration
GreenMark Biomedical Lab
FDA establishment registration 3020856747 · Ann Arbor, US
Key facts
| Registration number | 3020856747 |
|---|---|
| Establishment name | GreenMark Biomedical Lab |
| Owner/operator | GreenMark Biomedical Inc. |
| Owner/operator number | 10083206 |
| FEI number | 3020856747 |
| Address | 1600 Huron Parkway, Building 520, 2nd Floor |
| City | Ann Arbor |
| State | MI |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | EAQ, EJR, LFC |
| Device classes | 1, 2 |
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