FDA device listing
COSRX AC Collection Acne Patch,COSRX Acne Pimple Master Patch,COSRX Clear Fit Master Patch,COSRX Master Patch…
FDA device listing 1099449292 · COSRX
Key facts
| Proprietary names | COSRX AC Collection Acne Patch,COSRX Acne Pimple Master Patch,COSRX Clear Fit Master Patch,COSRX Master Patch Basic,COSRX Master Patch Clear Fit,COSRX Master Patch Intensive,COSRX Master Patch Original Fit,COSRX Master Patch Set,COSRX Master Patch X-Large |
|---|---|
| Owner/operator | COSRX |
| Owner/operator number | 10076803 |
| Product codes | NAD |
| Device names | NAD - Dressing, Wound, Occlusive |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4020 |
| Review panels | General & Plastic Surgery |
| Registered establishments | COSRX INC |
| Establishment registrations | 3021103089 |
| FEI numbers | 3021103089 |
| Establishment operations | 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