FDA device listing
5 ml and 10 ml Thrombin FSP pouch (Thrombin vial with Vial Access Device); Floseal,Floseal,FloSeal Endoscopic…
FDA device listing 1063681047 · Sotera Health LLC
Key facts
| Proprietary names | 5 ml and 10 ml Thrombin FSP pouch (Thrombin vial with Vial Access Device); Floseal,Floseal,FloSeal Endoscopic Applicator,Floseal Hemostatic Matrix,FLOSEAL HEMOSTATIC MATRIX,Floseal Hemostatic Matrix, 10mL, Six-Pack,Floseal Hemostatic Matrix, Six-Pack, 5cc,Floseal Hemostatic Matrix VH S/D, 10mL, Needle-Free. U.S., Fast Prep 2.0 Configuration Six Pack,Floseal Hemostatic Matrix VH S/D, 10mL… |
|---|---|
| Owner/operator | Sotera Health LLC |
| Owner/operator number | 10029425 |
| Product codes | LMF, PMX |
| Device names | LMF - Agent, Absorbable Hemostatic, Collagen Based, PMX - Absorbable Collagen Hemostatic Agent With Thrombin |
| Device class | Class III |
| Classification regulations (21 CFR) | 878.4490 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Sterigenics U.S. LLC, Sterigenics U.S., LLC, Sterigenics US LLC |
| Establishment registrations | 2011171, 2029275, 2953359, 3002907620 |
| FEI numbers | 2011171, 1000306431, 3000215205, 3002907620 |
| 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