Data / Medical devices / Monitor, Ultrasonic, Fetal / United States
FDA-registered makers of Monitor, Ultrasonic, Fetal in the United States: 6 establishments
6 establishments in the United States are registered with the FDA to make Monitor, Ultrasonic, Fetal (product code KNG). 4 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
- Monitor, Ultrasonic, Fetal
- Product code
- KNG
- Country
- United States
Makers of Monitor, Ultrasonic, Fetal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advanced Instrumentations, Inc. | Miami, FL, United States | Manufacturer | 2 | October 27, 2011 | 0 | 0 | 0 | api.fda.gov |
| Coopersurgical, Inc. | Trumbull, CT, United States | Manufacturer | 2 | January 3, 2003 | 0 | 1 | 0 | api.fda.gov |
| B'orze Inc | Boise, ID, United States | Specification developer | 1 | March 1, 2019 | 0 | 0 | 0 | api.fda.gov |
| Imex, LLC | Fulton, MD, United States | Manufacturer | 1 | July 2, 1990 | 0 | 0 | 0 | api.fda.gov |
| EDAN Diagnostics, Inc. | San Diego, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Natus Neurology Incorporated | Middleton, WI, United States | 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.