FDA device listing
Bausch & Lomb Ultra for Astigmatism,Bausch & Lomb Ultra for Presbyopia,Bausch & Lomb Ultra Multifocal for…
FDA device listing 1793869157 · ANGEL EYE CENTRE LTD.
Key facts
| Proprietary names | Bausch & Lomb Ultra for Astigmatism,Bausch & Lomb Ultra for Presbyopia,Bausch & Lomb Ultra Multifocal for Astigmatism,ULTRA DW |
|---|---|
| Owner/operator | ANGEL EYE CENTRE LTD. |
| Owner/operator number | 10046533 |
| Premarket submissions | K182249 |
| Product codes | LPL, MVN |
| Device names | LPL - Lenses, Soft Contact, Daily Wear, MVN - Lens, Contact, (Disposable) |
| Device class | Class II |
| Classification regulations (21 CFR) | 886.5925 |
| Review panels | Ophthalmic |
| Registered establishments | ANGEL EYE CENTRE LTD. |
| Establishment registrations | 3010890435 |
| FEI numbers | 3010890435 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes 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