Data / Medical devices / Filters, Cell Collection, Tissue Processing / United States
FDA-registered makers of Filters, Cell Collection, Tissue Processing in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make Filters, Cell Collection, Tissue Processing (product code KET). 0 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
- Filters, Cell Collection, Tissue Processing
- Product code
- KET
- Country
- United States
Makers of Filters, Cell Collection, Tissue Processing in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioseal | Placentia, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Becton, Dickinson and Company | Mebane, NC, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomedical Polymers, Inc. | Sterling, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cellsolutions LLC | Greensboro, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cole Instruments | Alpharetta, GA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caplugs, Inc. | Rancho Dominguez, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fisher Diagnostics | Middletown, VA, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hologic, Inc. | Marlborough, MA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Highridge Medical, LLC | Westminster, CO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hologic, Inc. | Marlborough, MA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hologic, Inc. | Londonderry, NH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kmi Imi Group / Dba: Innovative Med, Inc. | Irvine, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Leavitt Medical, Inc. | Lehi, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Omnia Inventa Medical, Inc. | San Diego, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Olive Branch Distribution Center | Olive Branch, MS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ranfac Corp. | Avon, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wavesense, Inc. | Irvine, CA, United States | 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.