Data / Medical devices / Punch, Femoral Neck / United States

FDA-registered makers of Punch, Femoral Neck in the United States: 22 establishments

Name: FDA-registered makers of Punch, Femoral Neck in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

22 establishments in the United States are registered with the FDA to make Punch, Femoral Neck (product code HWP). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in the United States Watch these makers

Device: Punch, Femoral Neck
Product code: HWP
Country: United States

Makers of Punch, Femoral Neck in the United States

Maker	Location	Role	Source
Biomet, Inc.	Warsaw, IN, United States	Manufacturer	api.fda.gov
Bradshaw Medical Inc.	Kenosha, WI, United States	Contract manufacturer, Manufacturer	api.fda.gov
C+a Tool Engineering, Inc.	Churubusco, IN, United States	Contract manufacturer	api.fda.gov
Culver Tool & Engineering	Plymouth, IN, United States	Contract manufacturer	api.fda.gov
Depuy Spine, Inc.	Raynham, MA, United States	Specification developer	api.fda.gov
Dunamis Medical LLC	Greenville, AL, United States	Manufacturer, Specification developer	api.fda.gov
Exactech, Inc.	Gainesville, FL, United States	Manufacturer	api.fda.gov
Innomed, Inc.	Savannah, GA, United States	Repackager or relabeler, Specification developer	api.fda.gov
Instrumental Machine & Development, Inc.	Warsaw, IN, United States	Contract manufacturer	api.fda.gov
Maitland Engineering	South Bend, IN, United States	Contract manufacturer	api.fda.gov
Microport Orthopedics Inc.	Arlington, TN, United States	Repackager or relabeler, Specification developer	api.fda.gov
Metal Craft Machine & Engineering, Inc.	Elk River, MN, United States	Contract manufacturer	api.fda.gov
Millstone Medical Outsourcing LLC	Olive Branch, MS, United States	Contract manufacturer	api.fda.gov
Nanova Biomaterials Inc	Columbia, MO, United States	Manufacturer, Specification developer	api.fda.gov
Riverside Machine & Engineering, Inc.	Eau Claire, WI, United States	Contract manufacturer	api.fda.gov
Summit MFG. And Machining, Inc.	Bremen, IN, United States	Contract manufacturer	api.fda.gov
Symmetry Medical Manufacturing Inc	Claypool, IN, United States	Contract manufacturer, Manufacturer	api.fda.gov
Symmetry Medical Manufacturing Inc.	Warsaw, IN, United States	Contract manufacturer, Manufacturer	api.fda.gov
UOC USA Inc.	Irvine, CA, United States	Manufacturer, Manufacturer for export	api.fda.gov
Wright Medical Technology, Inc.	Arlington, TN, United States	Manufacturer	api.fda.gov
Wright Medical Technology, Inc.	Arlington, TN, United States	Complaint file establishment, Specification developer	api.fda.gov
Zimmer, Inc.	Warsaw, IN, United States	Manufacturer	api.fda.gov

Updated November 3, 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.