Establishment registration
BINDER LIFT Inc.DBA PHASE
FDA establishment registration 3019991551 · Bigfork, US
Key facts
| Registration number | 3019991551 |
|---|---|
| Establishment name | BINDER LIFT Inc.DBA PHASE |
| Owner/operator | Binder Lift dba Phase |
| Owner/operator number | 10090211 |
| FEI number | 3019991551 |
| Address | 963 Blue Lake Ln |
| City | Bigfork |
| State | MT |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | FMR, FPP, IKX |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None 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