Data / Medical devices / Analyzer, Body Composition / United States
FDA-registered makers of Analyzer, Body Composition in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Analyzer, Body Composition (product code MNW). 3 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
- Analyzer, Body Composition
- Product code
- MNW
- Country
- United States
Makers of Analyzer, Body Composition in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Higi SH LLC | Chicago, IL, United States | Specification developer | 2 | January 26, 2011 | 0 | 0 | 0 | api.fda.gov |
| Fitbit LLC | San Francisco, CA, United States | Manufacturer | 1 | June 2, 2014 | 0 | 0 | 0 | api.fda.gov |
| LD Technology LLC | Miami, FL, United States | Specification developer | 1 | March 29, 2011 | 0 | 0 | 0 | api.fda.gov |
| Csa Service Solutions, LLC | Wilmington, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Impedimed, Inc. | Carlsbad, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| OnCore Manufacturing | Westborough, 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.