FDA device listing
Agent, Absorbable Hemostatic, Collagen Based
FDA device listing 1035273546 · Lyophilization Services of New England, Inc.
Key facts
| Owner/operator | Lyophilization Services of New England, Inc. |
|---|---|
| Owner/operator number | 9031362 |
| 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 | LYOPHILIZATION SERVICES OF NEW ENGLAND, INC. |
| Establishment registrations | 1225991 |
| FEI numbers | 3002516348 |
| 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