Establishment registration
ORTHO ORGANIZERS, INC.
FDA establishment registration 2081322 · Savannah, US
Key facts
| Registration number | 2081322 |
|---|---|
| Establishment name | ORTHO ORGANIZERS, INC. |
| Owner/operator | ORTHO ORGANIZERS , INC. |
| Owner/operator number | 2081322 |
| FEI number | 2081322 |
| Address | 800 King George Blvd, Suite 100 |
| City | Savannah |
| State | GA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DYJ, DYT, DYW, DZB, DZC, DZD, DZN, EAX, ECI, ECM, ECN, ECO, ECP, ECQ, ECR, ECS, EFT, EFW, EGD, EHJ, EHM, EHP, EHY, EIG, EIL, EJB, EJF, EJL, EJR, ELW and 10 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 1,000+ 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