FDA device listing
DORC10527 (PL) - hacoemulsification / Vitrectomy System / Ophthalmic Laser,DORC10527 (PL) - Instrument, vitreous…
FDA device listing 2028455377 · STERIS Corporation
Key facts
| Proprietary names | DORC10527 (PL) - hacoemulsification / Vitrectomy System / Ophthalmic Laser,DORC10527 (PL) - Instrument, vitreous aspiration and cutting, AC-powered,DORC10527 (PL) - Phacoemulsification/Vitrectomy System,DORC10527 (PL) - unit, phacofragmentation |
|---|---|
| Owner/operator | STERIS Corporation |
| Owner/operator number | 9072619 |
| 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 | Isomedix Operations Inc. |
| Establishment registrations | 2246552 |
| FEI numbers | 2246552 |
| Establishment operations | Contract Sterilizer |
| 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