Establishment registration
Reflow Medical
FDA establishment registration 3027058844 · Lake Forest, US
Key facts
| Registration number | 3027058844 |
|---|---|
| Establishment name | Reflow Medical |
| Owner/operator | Reflow Medical |
| Owner/operator number | 10034685 |
| FEI number | 3027058844 |
| Address | 20532 Crescent Bay Dr. Suite 100 |
| City | Lake Forest |
| State | CA |
| Country | US |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | DQY, PDU, SEU |
| Device classes | 2 |
At a glance
- 10–99 Device listings
- 10–99 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