FDA device listing
ESENTA Sting Free Skin Barrier Foam Applicators,ESENTA Sting Free Skin Barrier Pump Spray,ESENTA Sting Free Skin Barrier…
FDA device listing 1040252185 · ConvaTec
Key facts
| Proprietary names | ESENTA Sting Free Skin Barrier Foam Applicators,ESENTA Sting Free Skin Barrier Pump Spray,ESENTA Sting Free Skin Barrier Spray,ESENTA Sting Free Skin Barrier Wipes,SENSI-CARE Skin Barrier Foam Applicators,SENSI-CARE Skin Barrier Spray,SENSI-CARE Skin Barrier Wipes,Trio Silesse |
|---|---|
| Owner/operator | ConvaTec |
| Owner/operator number | 2241599 |
| Product codes | NEC |
| Device names | NEC - Bandage, Liquid, Skin Protectant |
| Device class | Class I |
| Classification regulations (21 CFR) | 880.5090 |
| Review panels | General Hospital |
| Registered establishments | ConvaTec, Inc., ConvaTec Limited, GDC Building |
| Establishment registrations | 3008806809, 3011987967 |
| FEI numbers | 3008806809, 3011987967 |
| Establishment operations | Complaint File Establishment, 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