Data / Medical devices / Container, Specimen Mailer And Storage, Sterile / United States

FDA-registered makers of Container, Specimen Mailer And Storage, Sterile in the United States: 21 establishments

Name: FDA-registered makers of Container, Specimen Mailer And Storage, Sterile in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in the United States are registered with the FDA to make Container, Specimen Mailer And Storage, Sterile (product code KDT). 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: Container, Specimen Mailer And Storage, Sterile
Product code: KDT
Country: United States

Makers of Container, Specimen Mailer And Storage, Sterile in the United States

Maker	Location	Role	Source
Alphapointe	Kansas City, MO, United States	Manufacturer	api.fda.gov
Becton Dickinson	Franklin Lakes, NJ, United States	Specification developer	api.fda.gov
Becton, Dickinson & Co.	Broken Bow, NE, United States	Manufacturer	api.fda.gov
Biomedical Polymers, Inc.	Sterling, MA, United States	Manufacturer	api.fda.gov
Cardinal Health 200, LLC	Jacksonville, TX, United States	Manufacturer	api.fda.gov
Copan Diagnostics, Inc.	Murrieta, CA, United States	Manufacturer	api.fda.gov
COPAN Diagnostics, Inc.	Carlsbad, CA, United States	Manufacturer	api.fda.gov
CalibreScientific US, Inc.	Vancouver, WA, United States	Manufacturer	api.fda.gov
Caplugs, Inc.	Rancho Dominguez, CA, United States	Manufacturer	api.fda.gov
Cardinal Health	Hazelwood, MO, United States	Specification developer	api.fda.gov
Fellow Health Inc.	San Leandro, CA, United States	Manufacturer	api.fda.gov
Geotec, Inc.	Warwick, RI, United States	Contract manufacturer	api.fda.gov
Labcon, North America	Petaluma, CA, United States	Contract manufacturer, Manufacturer	api.fda.gov
Labone, Inc.	Lenexa, KS, United States	Specification developer	api.fda.gov
Medical Chemical Corporation	Torrance, CA, United States	Manufacturer, Repackager or relabeler	api.fda.gov
Meridian Bioscience, Inc.	Cincinnati, OH, United States	Manufacturer	api.fda.gov
Rsi Technology Group, LLC	Frisco, TX, United States	Specification developer	api.fda.gov
Sarstedt, Inc.	Newton, NC, United States	Manufacturer	api.fda.gov
Somavac Medical Solutions, Inc.	Memphis, TN, United States	Manufacturer	api.fda.gov
Springside Scientific LLC	Durham, NC, United States	Repackager or relabeler, Specification developer	api.fda.gov
STS Corporation	Duluth, GA, United States	Complaint file establishment, Repackager or relabeler, Specification developer	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.