Data / Medical devices / Agent, Absorbable Hemostatic, Collagen Based / United States
FDA-registered makers of Agent, Absorbable Hemostatic, Collagen Based in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Agent, Absorbable Hemostatic, Collagen Based (product code LMF). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Agent, Absorbable Hemostatic, Collagen Based
- Product code
- LMF
- Country
- United States
Makers of Agent, Absorbable Hemostatic, Collagen Based in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Davol Inc. | Woburn, MA, United States | Manufacturer | 0 | 2 | 0 | 0 | api.fda.gov | |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI, United States | Complaint file establishment, Specification developer | 0 | 2 | 1 | 0 | api.fda.gov | |
| Integra Lifesciences Corporation | Plainsboro, NJ, United States | Manufacturer | 0 | 1 | 1 | 0 | api.fda.gov | |
| Integra Neurosciences | Anasco, PR, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Integra LifeSciences Corporation | Princeton, NJ, United States | Complaint file establishment, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Baxter Healthcare Corporation | Hayward, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lyophilization Services Of New England, Inc. | Manchester, NH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vascular Solutions LLC | Maple Grove, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.