Data / Medical devices / Dc-Defibrillator, Low-Energy, (Including Paddles) / United States
FDA-registered makers of Dc-Defibrillator, Low-Energy, (Including Paddles) in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Dc-Defibrillator, Low-Energy, (Including Paddles) (product code LDD). 7 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Dc-Defibrillator, Low-Energy, (Including Paddles)
- Product code
- LDD
- Country
- United States
Makers of Dc-Defibrillator, Low-Energy, (Including Paddles) in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Cardio Medical Products, Inc. | Rockaway, NJ, United States | Specification developer | 3 | October 4, 2011 | 0 | 1 | 0 | api.fda.gov |
| Unipower Corp. | Minnetonka, MN, United States | Manufacturer | 2 | September 7, 1994 | 0 | 0 | 0 | api.fda.gov |
| Zoll Medical Corporation | Chelmsford, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 2 | July 29, 2010 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Westborough, MA, United States | Specification developer | 1 | December 11, 1996 | 0 | 0 | 0 | api.fda.gov |
| Graphic Controls Acquisition Corp.dba Nissha Medical Technologies | Buffalo, NY, United States | Specification developer | 1 | September 24, 2008 | 0 | 0 | 0 | api.fda.gov |
| Physio-Control, Inc. | Redmond, WA, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | June 3, 2019 | 0 | 14 | 0 | api.fda.gov |
| Philips North America LLC | Bothell, WA, United States | Specification developer | 1 | January 11, 2021 | 0 | 0 | 0 | api.fda.gov |
| Advanced Instrumentations, Inc. | Miami, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anybattery, Inc | Rosemount, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Katecho LLC | Des Moines, IA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scientific Molding Corporation, Ltd. Dba SMC Ltd. | Somerset, WI, 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.