FDA device listing
FarrowHybrid ADI Foot Compression
FDA device listing 1848513985 · Blue Lagoon Inc. dba Tec-Ops
Key facts
| Proprietary names | FarrowHybrid ADI Foot Compression |
|---|---|
| Owner/operator | Blue Lagoon Inc. dba Tec-Ops |
| Owner/operator number | 10088209 |
| Product codes | MDR |
| Device names | MDR - Binder, Medical, Therapeutic |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5160 |
| Review panels | General Hospital |
| Registered establishments | BLUE LAGOON INC. DBA TEC-OPS |
| Establishment registrations | 3027484200 |
| FEI numbers | 3027484200 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database