FDA device listing
bowman lacrimal probe, sterling, 5 1/8 (13.0 cm), sterling, size 00-0,bowman lacrimal probe, sterling, 5 1/8 (13.0 cm)…
FDA device listing 1580963507 · ALFRAMED
Key facts
| Proprietary names | bowman lacrimal probe, sterling, 5 1/8 (13.0 cm), sterling, size 00-0,bowman lacrimal probe, sterling, 5 1/8 (13.0 cm), sterling, size 0000-000,bowman lacrimal probe, sterling, 5 1/8 (13.0 cm), sterling, size 1-2,quickert lacrimal intubation probe, size 3 |
|---|---|
| Owner/operator | ALFRAMED |
| Owner/operator number | 10049091 |
| Product codes | HNL |
| Device names | HNL - Probe, Lachrymal |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4350 |
| Review panels | Ophthalmic |
| Registered establishments | ALFRAMED |
| Establishment registrations | 3010699884 |
| FEI numbers | 3010699884 |
| Establishment operations | Foreign Exporter, 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