Data / Medical devices / Compressor, Cardiac, External / United States
FDA-registered makers of Compressor, Cardiac, External in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Compressor, Cardiac, External (product code DRM). 5 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Compressor, Cardiac, External
- Product code
- DRM
- Country
- United States
Makers of Compressor, Cardiac, External in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| ZOLL Circulation, Inc. | San Jose, CA, United States | Complaint file establishment, Manufacturer | 4 | March 9, 2023 | 0 | 5 | 1 | api.fda.gov |
| Defibtech, LLC | Guilford, CT, United States | Specification developer | 2 | November 9, 2021 | 0 | 1 | 1 | api.fda.gov |
| Defibtech Branford | Branford, CT, United States | Manufacturer | 2 | November 9, 2021 | 0 | 0 | 0 | api.fda.gov |
| Defibtech North Branford | North Branford, CT, United States | Manufacturer | 2 | November 9, 2021 | 0 | 0 | 0 | api.fda.gov |
| Michigan Instruments | Grand Rapids, MI, United States | Manufacturer, Manufacturer for export | 2 | February 14, 2008 | 0 | 3 | 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.