Data / Medical devices / Tray, Biopsy, Without Biopsy Instruments / United States
FDA-registered makers of Tray, Biopsy, Without Biopsy Instruments in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Tray, Biopsy, Without Biopsy Instruments (product code FCH). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Tray, Biopsy, Without Biopsy Instruments
- Product code
- FCH
- Country
- United States
Makers of Tray, Biopsy, Without Biopsy Instruments in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Avid Medical, Inc. A Medical Action Ind. Company 305 | Toano, VA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Busse Hospital Disposables | Hauppauge, NY, United States | Manufacturer, Manufacturer for export, Repackager or relabeler | 0 | 0 | 2 | 0 | api.fda.gov | |
| Devicor Medical Products, Inc. | Cincinnati, OH, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Diversatek Healthcare Inc | Milwaukee, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dynamic Diagnostics Incorporated | Plymouth, MI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HK Surgical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Laredo | Laredo, TX, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medline Industries, LP - SPT | Waukegan, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trinity Sterile, Inc. | Salisbury, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therapak, LLC | Oakwood, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Uramix, Inc. | E Lansdowne, PA, United States | Specification developer | 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.