FDA device listing
Absorbable hemosatic agent and dressing Vitagel Surgical Hemostat CellPaker Collection Device,Absorbable hemosatic agent…
FDA device listing 1887151842 · Sotera Health LLC
Key facts
| Proprietary names | Absorbable hemosatic agent and dressing Vitagel Surgical Hemostat CellPaker Collection Device,Absorbable hemosatic agent and dressing Vitagel Surgical Hemostat Malleable Extended Applicator (MEA) |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | LMF |
| Device names | LMF - Agent, Absorbable Hemostatic, Collagen Based |
| Device class | Class III |
| Classification regulations (21 CFR) | 878.4490 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Sterigenics Radiation Technologies, LLC |
| Establishment registrations | 2024024 |
| FEI numbers | 2024024 |
| 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