Data / Medical devices / Agent, Absorbable Hemostatic, Non-Collagen Based / United States
FDA-registered makers of Agent, Absorbable Hemostatic, Non-Collagen Based in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Agent, Absorbable Hemostatic, Non-Collagen Based (product code LMG). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Agent, Absorbable Hemostatic, Non-Collagen Based
- Product code
- LMG
- Country
- United States
Makers of Agent, Absorbable Hemostatic, Non-Collagen Based in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Baxter Healthcare Corporation | Round Lake, IL, United States | Complaint file establishment, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Davol Inc. | Woburn, MA, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI, United States | Complaint file establishment, Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, Inc. | Somerville, NJ, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, Inc. | Raritan, NJ, United States | Specification developer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Ethicon, LLC. | San Lorenzo, PR, United States | Manufacturer | 0 | 1 | 0 | 0 | api.fda.gov | |
| Alltrista Plastics LLC | Reedsville, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Artivion, Inc. | Kennesaw, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Clayens Fitchburg, Ma | Fitchburg, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | North Haven, CT, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | Northborough, MA, United States | Contract sterilizer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgical Technologies, Inc. | St. Paul, 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.