Data / Medical devices / Clamp, Vascular / United States
FDA-registered makers of Clamp, Vascular in the United States: 63 establishments
63 establishments in the United States are registered with the FDA to make Clamp, Vascular (product code DXC). 44 have a 510(k) clearance or PMA approval on file and 7 have a recall event. FDA data exported November 2, 2026.
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- Device
- Clamp, Vascular
- Product code
- DXC
- Country
- United States
Makers of Clamp, Vascular in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Advanced Vascular Dynamics | Tigard, OR, United States | Manufacturer, Specification developer | 13 | July 31, 2015 | 0 | 0 | 0 | api.fda.gov |
| Applied Medical Resources Corp. | Rsm, CA, United States | Complaint file establishment, Manufacturer | 8 | January 8, 2001 | 0 | 1 | 0 | api.fda.gov |
| Applied Medical Distribution Center | Irvine, CA, United States | Manufacturer | 8 | January 8, 2001 | 0 | 0 | 0 | api.fda.gov |
| Enablecv, LLC | Midvale, UT, United States | Specification developer | 7 | January 26, 2017 | 0 | 0 | 0 | api.fda.gov |
| STERIS Corporation | Saint Louis, MO, United States | Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer | 6 | March 4, 2021 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 6 | October 23, 2014 | 0 | 0 | 0 | api.fda.gov |
| Vitalitec Int'l., Inc. | Plymouth, MA, United States | Specification developer | 5 | September 5, 2003 | 0 | 0 | 0 | api.fda.gov |
| Merit Medical Systems, Inc. | South Jordan, UT, United States | Manufacturer, Specification developer | 4 | April 17, 2018 | 0 | 2 | 0 | api.fda.gov |
| TZ Medical, Inc. | Tualatin, OR, United States | Manufacturer, Specification developer | 4 | January 10, 2018 | 0 | 0 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 4 | October 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Becton, Dickinson And Company | Irvine, CA, United States | Specification developer | 3 | June 5, 2026 | 0 | 0 | 0 | api.fda.gov |
| Edwards Lifesciences Technology Sarl | Anasco, PR, United States | Manufacturer | 3 | June 5, 2026 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 3 | November 20, 2025 | 0 | 0 | 0 | api.fda.gov |
| SYNOVIS LIFE TECHNOLOGIES, INC. (A Subsidiary of Baxter International Inc.) | Saint Paul, MN, United States | Manufacturer | 3 | September 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| Argon Medical Devices Inc. | Athens, TX, United States | Manufacturer, Repackager or relabeler | 2 | July 9, 1998 | 0 | 0 | 0 | api.fda.gov |
| Aros Surgical Instruments Corporation | North Wales, PA, United States | Specification developer | 2 | August 18, 2016 | 0 | 0 | 0 | api.fda.gov |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 2 | October 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Instrumed International Inc dba Avalign German Specialty Instruments | Schaumburg, IL, United States | Contract manufacturer, Repackager or relabeler | 2 | October 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Marine Polymer Technologies, Inc. | Topsfield, MA, United States | Manufacturer | 2 | July 31, 2014 | 0 | 0 | 0 | api.fda.gov |
| Maquet Cardiovascular LLC | Wayne, NJ, United States | Manufacturer | 2 | June 5, 2013 | 0 | 2 | 0 | api.fda.gov |
| Terumo Medical Corp. | Elkton, MD, United States | Manufacturer | 2 | December 20, 2021 | 0 | 0 | 0 | api.fda.gov |
| Vascular Solutions LLC | Maple Grove, MN, United States | Manufacturer, Repackager or relabeler | 2 | September 27, 2011 | 0 | 0 | 0 | api.fda.gov |
| AVALIGN TECHNOLOGIES, Inc. | Fort Wayne, IN, United States | Specification developer | 1 | October 26, 2009 | 0 | 0 | 0 | api.fda.gov |
| Abbott Medical | Caguas, PR, United States | Manufacturer, Manufacturer for export | 1 | February 24, 2011 | 0 | 0 | 0 | api.fda.gov |
| Compression Works Inc. | Birmingham, AL, United States | Complaint file establishment, Specification developer | 1 | March 3, 2023 | 0 | 0 | 0 | api.fda.gov |
| Edwards Lifesciences LLC | Irvine, CA, United States | Specification developer | 1 | May 16, 1991 | 0 | 2 | 1 | api.fda.gov |
| Ensitevascular, LLC | Overland Park, KS, United States | Complaint file establishment, Specification developer | 1 | March 31, 2020 | 0 | 0 | 0 | api.fda.gov |
| Edwards Lifesciences LLC | Draper, UT, United States | Manufacturer | 1 | May 16, 1991 | 0 | 4 | 0 | api.fda.gov |
| Fetzer Surgical, LLC | Scottsdale, AZ, United States | Repackager or relabeler, Specification developer | 1 | April 30, 2012 | 0 | 0 | 0 | api.fda.gov |
| HeartStitch, INC. | Fountain Valley, CA, United States | Manufacturer | 1 | July 24, 1998 | 0 | 0 | 0 | api.fda.gov |
| Innovative Trauma Care Inc | San Antonio, TX, United States | Complaint file establishment, Specification developer | 1 | April 30, 2015 | 0 | 0 | 0 | api.fda.gov |
| MML Diagnostics Packaging, Inc. | Troutdale, OR, United States | Contract manufacturer, Repackager or relabeler | 1 | December 11, 1997 | 0 | 0 | 0 | api.fda.gov |
| North American Rescue, LLC. | Greer, SC, United States | Manufacturer | 1 | January 3, 2013 | 0 | 1 | 0 | api.fda.gov |
| Novosci Corp. | Conroe, TX, United States | Manufacturer, Specification developer | 1 | June 30, 1980 | 0 | 0 | 0 | api.fda.gov |
| Nobles Medical Technologies II, Inc. | Fountain Valley, CA, United States | Specification developer | 1 | July 24, 1998 | 0 | 0 | 0 | api.fda.gov |
| Safeguard Us Operating, LLC | Huntersville, NC, United States | Specification developer | 1 | August 11, 2010 | 0 | 0 | 0 | api.fda.gov |
| Sam Medical Products | Tualatin, OR, United States | Manufacturer | 1 | July 24, 2013 | 0 | 1 | 0 | api.fda.gov |
| SYNOVIS MICRO COMPANIES ALLIANCE, INC. (a subsidiary of Baxter International Inc.) | Birmingham, AL, United States | Specification developer | 1 | September 14, 2022 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical | Roseville, MN, United States | Manufacturer | 1 | February 24, 2011 | 0 | 0 | 0 | api.fda.gov |
| St. Jude Medical, Cardiology Division, Inc. | Plymouth, MN, United States | Manufacturer | 1 | February 24, 2011 | 0 | 0 | 0 | api.fda.gov |
| Vasoinnovations Inc. | South Pasadena, CA, United States | Manufacturer | 1 | March 14, 2019 | 0 | 0 | 0 | api.fda.gov |
| Vitalcor, Inc. | Westmont, IL, United States | Specification developer | 1 | August 29, 2007 | 0 | 0 | 0 | api.fda.gov |
| Wexler Surgical, Inc. | Houston, TX, United States | Repackager or relabeler, Specification developer | 1 | April 19, 2011 | 0 | 0 | 0 | api.fda.gov |
| voss medical products | San Antonio, TX, United States | Manufacturer | 1 | December 22, 1989 | 0 | 0 | 0 | api.fda.gov |
| Advanced Concept Innovations LLC | Lakeland, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biomerics | Salt Lake City, UT, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Biorep Technologies, Inc. | Miami Lakes, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dielectrics, Inc. | Chicopee, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Gilero, Inc | Pittsboro, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Harwood Design, Inc. | Bristol, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JLP Machine And Welding LLC | Kingston, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kapp Surgical, Inc. | Cleveland, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lyophilization Services Of New England, Inc. | Manchester, NH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medbio, LLC. | Grand Rapids, MI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medical Components Inc | Harleysville, PA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MME Willow Lake | Vadnais Hts, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phoenix Instruments, Inc. | Lisle, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Polo Custom Products | Louisville, MS, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Polo Custom Products | Monticello, IA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Scanlan International, Inc. | Saint Paul, MN, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Springboard Manufacturing | Rancho Cordova, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Trident Manufacturing, Inc. | Pingree Grove, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wright Engineered Plastics, Inc. | Santa Rosa, CA, 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.