Data / Medical devices / Device, Microtiter Diluting/Dispensing / United States
FDA-registered makers of Device, Microtiter Diluting/Dispensing in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Device, Microtiter Diluting/Dispensing (product code JTC). 2 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
- Device, Microtiter Diluting/Dispensing
- Product code
- JTC
- Country
- United States
Makers of Device, Microtiter Diluting/Dispensing in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Diagnostic Automation/ Cortez Diagnostics Inc,. | Woodland Hills, CA, United States | Manufacturer | 1 | December 2, 1988 | 0 | 0 | 0 | api.fda.gov |
| Remel, Inc. | Lenexa, KS, United States | Specification developer | 1 | July 21, 1980 | 0 | 0 | 0 | api.fda.gov |
| Beckman Coulter, Inc. | Miami, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Becton, Dickinson & Co. | Sparks, MD, United States | Complaint file establishment, Manufacturer | 0 | 0 | 2 | 0 | api.fda.gov | |
| Beckman Coulter, Inc. | West Sacramento, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Caplugs, Inc. | Rancho Dominguez, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hamilton Co. | Reno, NV, United States | Contract manufacturer | 0 | 0 | 4 | 0 | api.fda.gov | |
| Plastikon Industries | Hayward, CA, 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.