Data / Medical devices / Massager, Vacuum, Radio Frequency Induced Heat / United States
FDA-registered makers of Massager, Vacuum, Radio Frequency Induced Heat in the United States: 12 establishments
12 establishments in the United States are registered with the FDA to make Massager, Vacuum, Radio Frequency Induced Heat (product code PBX). 9 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
- Massager, Vacuum, Radio Frequency Induced Heat
- Product code
- PBX
- Country
- United States
Makers of Massager, Vacuum, Radio Frequency Induced Heat in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Venus Concept Inc. | San Jose, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 4 | April 27, 2022 | 0 | 0 | 0 | api.fda.gov |
| Venus Concept Inc. | Windham, NH, United States | Complaint file establishment, Manufacturer, Specification developer | 4 | April 27, 2022 | 0 | 0 | 0 | api.fda.gov |
| Cynosure, LLC | Westford, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | March 25, 2020 | 0 | 0 | 0 | api.fda.gov |
| Heat In A Click LLC | Dania, FL, United States | Specification developer | 2 | September 26, 2022 | 0 | 0 | 0 | api.fda.gov |
| Cao Group, Inc. | W Jordan, UT, United States | Manufacturer | 1 | October 28, 2020 | 0 | 0 | 0 | api.fda.gov |
| Candela Corporation | Marlborough, MA, United States | Complaint file establishment, Specification developer | 1 | September 12, 2016 | 0 | 0 | 0 | api.fda.gov |
| General Vibronics, Inc. | Tempe, AZ, United States | Manufacturer | 1 | November 21, 2024 | 0 | 0 | 0 | api.fda.gov |
| Neauvia North America, Inc | Raleigh, NC, United States | Complaint file establishment, Specification developer | 1 | July 30, 2021 | 0 | 0 | 0 | api.fda.gov |
| XOD Inc | Philadelphia, PA, United States | Specification developer | 1 | February 27, 2025 | 0 | 0 | 0 | api.fda.gov |
| Cogmedix | West Boylston, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Express Manufacturing, Inc | Santa Ana, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Paragon Medical - Mansfield, Bridgemedica | Mansfield, MA, 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.