Data / Medical devices / Plethysmograph, Photoelectric, Pneumatic Or Hydraulic / United States
FDA-registered makers of Plethysmograph, Photoelectric, Pneumatic Or Hydraulic in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Plethysmograph, Photoelectric, Pneumatic Or Hydraulic (product code JOM). 4 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
- Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
- Product code
- JOM
- Country
- United States
Makers of Plethysmograph, Photoelectric, Pneumatic Or Hydraulic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Collaborative Care Diagnostics LLC dba BioMedix | Eagan, MN, United States | Complaint file establishment, Specification developer | 2 | October 20, 2022 | 0 | 0 | 0 | api.fda.gov |
| D. E. Hokanson, Inc. | Bellevue, WA, United States | Manufacturer | 2 | February 12, 2003 | 0 | 0 | 0 | api.fda.gov |
| LD Technology LLC | Miami, FL, United States | Manufacturer, Repackager or relabeler, Specification developer | 1 | December 19, 2017 | 0 | 0 | 0 | api.fda.gov |
| Semler Scientific, Inc. | Campbell, CA, United States | Manufacturer | 1 | March 5, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medeologix LLC | San Jose, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ontogen Manufacturing LLC | Lisle, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Parks Medical Electronics, Inc. | Aloha, OR, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PDV MedTech | Morgan Hill, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Philips North America LLC | Andover, MA, United States | 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.