Data / Medical devices / Mixer, Cement, For Clinical Use / United States

FDA-registered makers of Mixer, Cement, For Clinical Use in the United States: 27 establishments

Name: FDA-registered makers of Mixer, Cement, For Clinical Use in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

27 establishments in the United States are registered with the FDA to make Mixer, Cement, For Clinical Use (product code JDZ). 3 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: Mixer, Cement, For Clinical Use
Product code: JDZ
Country: United States

Makers of Mixer, Cement, For Clinical Use in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Depuy Orthopaedics, Inc.	Warsaw, IN, United States	Manufacturer, Specification developer	1	January 5, 1994	0	api.fda.gov
Stryker Puerto Rico, LLC.	Arroyo, PR, United States	Contract manufacturer, Manufacturer	1	August 29, 1991	0	api.fda.gov
Stryker Instruments	Portage, MI, United States	Complaint file establishment, Specification developer	1	August 29, 1991	0	api.fda.gov
Argon Medical Devices, Inc.	Wheeling, IL, United States	Contract manufacturer	0		0	api.fda.gov
Biomet, Inc.	Warsaw, IN, United States	Manufacturer	0		1	api.fda.gov
Cook Incorporated	Bloomington, IN, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Depuy Spine, Inc.	Raynham, MA, United States	Specification developer	0		0	api.fda.gov
DSM Biomedical, Inc.	Exton, PA, United States	Contract manufacturer	0		0	api.fda.gov
Globus Medical, Inc.	Audubon, PA, United States	Manufacturer	0		0	api.fda.gov
Globus Medical, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Izi Medical Products LLC	Owings Mills, MD, United States	Manufacturer	0		0	api.fda.gov
MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, United States	Specification developer	0		0	api.fda.gov
Medtronic Sofamor Danek Usa, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Medtronic Sofamor Danek Usa, Inc.	Memphis, TN, United States	Specification developer	0		0	api.fda.gov
Merit Medical Systems, Inc.	South Jordan, UT, United States	Manufacturer	0		0	api.fda.gov
Microport Orthopedics Inc.	Arlington, TN, United States	Manufacturer	0		0	api.fda.gov
Pulpdent Corporation	Watertown, MA, United States	Manufacturer	0		0	api.fda.gov
Quality Tech Services, LLC	Bloomington, MN, United States	Contract manufacturer	0		0	api.fda.gov
Ready Set Import	Beverly Hills, CA, United States	Specification developer	0		0	api.fda.gov
Smith & Nephew, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Stryker Manufacturing Kalamazoo	Portage, MI, United States	Contract manufacturer	0		0	api.fda.gov
Smith & Nephew, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Smith & Nephew, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Synthes (USA) Products LLC	West Chester, PA, United States	Specification developer	0		0	api.fda.gov
Zavation	Flowood, MS, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Zimmer Surgical, Inc.	Dover, OH, United States	Manufacturer	0		0	api.fda.gov
Zimmer, Inc.	Warsaw, IN, United States	Manufacturer	0		1	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.