FDA device listing
BL5723 23GA Light Pipe,BL5725 25GA Light Pipe,BL5820 20GA Wide Angle Light Pipe,BL5823 23GA Wide Angle Light Pipe,BL5825…
FDA device listing 1166825059 · PEREGRINE SURGICAL LLC
Key facts
| Proprietary names | BL5723 23GA Light Pipe,BL5725 25GA Light Pipe,BL5820 20GA Wide Angle Light Pipe,BL5823 23GA Wide Angle Light Pipe,BL5825 25GA Wide angle Light Pipe |
|---|---|
| Owner/operator | PEREGRINE SURGICAL LLC |
| Owner/operator number | 9002261 |
| Product codes | HQC, HQE, HQF |
| Device names | HQC - Unit, Phacofragmentation, HQE - Instrument, Vitreous Aspiration And Cutting, Ac-Powered, HQF - Laser, Ophthalmic |
| Device class | Class II |
| Classification regulations (21 CFR) | 886.4150, 886.4390, 886.4670 |
| Review panels | Ophthalmic |
| Registered establishments | Peregrine Surgical, LLC. |
| Establishment registrations | 2529392 |
| FEI numbers | 1000121498 |
| Establishment operations | Contract 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