Data / Medical devices / Apparatus, Suction, Ward Use, Portable, Ac-Powered / United States
FDA-registered makers of Apparatus, Suction, Ward Use, Portable, Ac-Powered in the United States: 27 establishments
27 establishments in the United States are registered with the FDA to make Apparatus, Suction, Ward Use, Portable, Ac-Powered (product code JCX). 16 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
- Apparatus, Suction, Ward Use, Portable, Ac-Powered
- Product code
- JCX
- Country
- United States
Makers of Apparatus, Suction, Ward Use, Portable, Ac-Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Instruments | Portage, MI, United States | Complaint file establishment, Specification developer | 3 | December 9, 2022 | 0 | 1 | 0 | api.fda.gov |
| Zimmer Surgical, Inc. | Dover, OH, United States | Manufacturer, Manufacturer for export, Specification developer | 3 | April 24, 2019 | 0 | 0 | 0 | api.fda.gov |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer, Specification developer | 2 | December 16, 2004 | 0 | 0 | 0 | api.fda.gov |
| Deroyal Industries, Inc. | Powell, TN, United States | Complaint file establishment, Specification developer | 1 | April 1, 2009 | 0 | 0 | 0 | api.fda.gov |
| DeVilbiss Healthcare LLC. | Somerset, PA, United States | Manufacturer | 1 | September 25, 1998 | 0 | 3 | 0 | api.fda.gov |
| Kmi Imi Group / Dba: Innovative Med, Inc. | Irvine, CA, United States | Manufacturer | 1 | October 18, 1989 | 0 | 0 | 0 | api.fda.gov |
| Micro Therapeutics, Inc. Dba Ev3 Neurovascular | Irvine, CA, United States | Specification developer | 1 | December 2, 2024 | 0 | 0 | 0 | api.fda.gov |
| Micro Therapeutics, Inc. Dba Ev3 Neurovascular | Irvine, CA, United States | Manufacturer | 1 | December 2, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medline ReNewal | Redmond, OR, United States | Reprocessor | 1 | August 3, 2017 | 0 | 0 | 0 | api.fda.gov |
| MicroVention, Inc. | Aliso Viejo, CA, United States | Specification developer | 1 | June 13, 2025 | 0 | 0 | 0 | api.fda.gov |
| Penumbra, Inc. | Alameda, CA, United States | Manufacturer | 1 | October 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Pneo, LLC | Denton, TX, United States | Complaint file establishment, Manufacturer, Repackager or relabeler | 1 | November 12, 2008 | 0 | 0 | 0 | api.fda.gov |
| Penumbra Inc. | Roseville, CA, United States | Manufacturer | 1 | October 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Penumbra Inc. | Salt Lake City, UT, United States | Manufacturer | 1 | October 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Penumbra Inc. | Livermore, CA, United States | Manufacturer | 1 | October 2, 2012 | 0 | 0 | 0 | api.fda.gov |
| Sscor, Inc. | Simi Valley, CA, United States | Manufacturer | 1 | July 24, 1979 | 0 | 0 | 0 | api.fda.gov |
| CPAC Equipment, Inc. | Leicester, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Deroyal Industries, Inc. | New Tazewell, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kimball Solutions - Indianapolis | Indianapolis, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kimball Solutions - Indianapolis | Indianapolis, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NBS Group Supply- Medical Products Division, LLC | New Brunswick, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Seacole-Crc, LLC | Plymouth, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Spartronics Strongsville, Inc. | Strongsville, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Manufacturing Kalamazoo | Portage, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Tessy Plastics Corp. | Elbridge, NY, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ultraviolet Devices, Inc. | Valencia, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vaupell Midwest Molding and Tooling | Constantine, MI, 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.