FDA device listing
Oleeva Clear,Oleeva Foam,Oleeva Ultra,ScarAway Silicone Scar Tape,Silon LTS,Silon STS,Silon-TEX II
FDA device listing 1310751958 · Wacker Silicone Manufactured Innovations LLC
Key facts
| Proprietary names | Oleeva Clear,Oleeva Foam,Oleeva Ultra,ScarAway Silicone Scar Tape,Silon LTS,Silon STS,Silon-TEX II |
|---|---|
| Owner/operator | Wacker Silicone Manufactured Innovations LLC |
| Owner/operator number | 10091011 |
| Product codes | MDA |
| Device names | MDA - Elastomer, Silicone, For Scar Management |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4025 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Wacker Silicone Manufactured Innovations LLC |
| Establishment registrations | 3031481777 |
| FEI numbers | 3031481777 |
| Establishment operations | Contract 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