Data / Medical devices / Manipulator, Plunger-Like Joint / United States
FDA-registered makers of Manipulator, Plunger-Like Joint in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Manipulator, Plunger-Like Joint (product code LXM). 9 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
- Manipulator, Plunger-Like Joint
- Product code
- LXM
- Country
- United States
Makers of Manipulator, Plunger-Like Joint in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Activator Methods International Ltd. | Phoenix, AZ, United States | Manufacturer | 3 | March 6, 2012 | 0 | 0 | 0 | api.fda.gov |
| Neuromechanical Innovations, LLC | Phoenix, AZ, United States | Manufacturer | 2 | April 11, 2008 | 0 | 0 | 0 | api.fda.gov |
| Hill Laboratories | Frazer, PA, United States | Manufacturer | 1 | June 20, 2018 | 0 | 0 | 0 | api.fda.gov |
| Integra LifeSciences Production Corporation | Mansfield, MA, United States | Manufacturer | 1 | April 30, 1996 | 0 | 0 | 0 | api.fda.gov |
| JTECH Medical Industries, Inc. | Midvale, UT, United States | Manufacturer | 1 | February 18, 1998 | 0 | 0 | 0 | api.fda.gov |
| Sense Technology, Inc. | Halifax, PA, United States | Manufacturer, Specification developer | 1 | June 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Sigma Instruments, Inc. | Cranberry Township, PA, United States | Manufacturer | 1 | January 10, 1997 | 0 | 0 | 0 | api.fda.gov |
| Spinalight Inc | St Petersburg, FL, United States | Manufacturer | 1 | June 20, 2018 | 0 | 1 | 0 | api.fda.gov |
| Sweat Institute | Atlanta, GA, United States | Manufacturer | 1 | November 21, 1995 | 0 | 0 | 0 | api.fda.gov |
| Hardy Manufacturing | Decatur, GA, 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.