Data / Medical devices / Device, Pressure Applying / United States
FDA-registered makers of Device, Pressure Applying in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Device, Pressure Applying (product code KNM). 0 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
- Device, Pressure Applying
- Product code
- KNM
- Country
- United States
Makers of Device, Pressure Applying in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Altimate Medical, Inc. | Frankfort, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashley Black Inc. | Houston, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Health Body World Supply, Inc. Dba The Wabbo Company | Lake Elsinore, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stetrix Inc. | Memphis, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Therabody, Inc. | Los Angeles, CA, United States | Complaint file establishment, Specification developer | 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.