FDA device listing
VisiGlide,VisiRing
FDA device listing 1087421682 · VISIONARY MEDICAL SUPPLIES, INC.
Key facts
| Proprietary names | VisiGlide,VisiRing |
|---|---|
| Owner/operator | VISIONARY MEDICAL SUPPLIES, INC. |
| Owner/operator number | 9040860 |
| Product codes | NCE |
| Device names | NCE - Injector, Capsular Tension Ring |
| Device class | Class I |
| Classification regulations (21 CFR) | 886.4300 |
| Review panels | Ophthalmic |
| Registered establishments | VISIONARY MEDICAL SUPPLIES, INC. |
| Establishment registrations | 1064514 |
| FEI numbers | 3004161528 |
| Establishment operations | Specification Developer, U.S. Manufacturer of Export Only Devices |
| 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