FDA device listing
HALYARD PROCEDURE GOWN
FDA device listing 1038501935 · O&M Halyard, Inc.
Key facts
| Proprietary names | HALYARD PROCEDURE GOWN |
|---|---|
| Owner/operator | O&M Halyard, Inc. |
| Owner/operator number | 10057479 |
| Product codes | LYU |
| Device names | LYU - Accessory, Surgical Apparel |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4040 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Halyard North Carolina, LLC, La Ada de Acuna, La Ada De Acuna, S. de. R. L. de C. V., O&M Halyard Honduras S.A de C.V., O&M Halyard, Inc. |
| Establishment registrations | 1054380, 9616096, 9680646, 3005997949, 3014421917 |
| FEI numbers | 1000110722, 1000582923, 3003807323, 3005997949, 3014421917 |
| Establishment operations | Complaint File Establishment, Manufacturer, Repackager/Relabeler, Specification Developer |
| 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