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Data / Medical devices / Electrode, Pacemaker, Temporary / United States

FDA-registered makers of Electrode, Pacemaker, Temporary in the United States: 27 establishments

27 establishments in the United States are registered with the FDA to make Electrode, Pacemaker, Temporary (product code LDF). 18 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Electrode, Pacemaker, Temporary
Product code
LDF
Country
United States

Makers of Electrode, Pacemaker, Temporary in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Oscor Inc.Palm Harbor, FL, United StatesComplaint file establishment, Manufacturer6January 22, 2008021api.fda.gov
Abbott MedicalMinnetonka, MN, United StatesManufacturer, Manufacturer for export4November 22, 2016000api.fda.gov
Becton, Dickinson And CompanyIrvine, CA, United StatesSpecification developer4October 15, 2015000api.fda.gov
Edwards Lifesciences Technology SarlAnasco, PR, United StatesManufacturer4October 15, 2015000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler3October 17, 1996000api.fda.gov
Abbott VascularSanta Clara, CA, United StatesSpecification developer2November 22, 2016000api.fda.gov
Alto Development Corp.Farmingdale, NJ, United StatesManufacturer2July 12, 2004020api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesContract sterilizer, Specification developer2May 15, 2025000api.fda.gov
Medtronic, Inc.Mounds View, MN, United StatesSpecification developer2May 26, 1998010api.fda.gov
Medtronic Heart Valves DivisionSanta Ana, CA, United StatesSpecification developer2August 8, 2019000api.fda.gov
St. Jude MedicalRoseville, MN, United StatesManufacturer2January 27, 1992000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer2November 3, 1987000api.fda.gov
Arrow International, LLC (subsidiary of Teleflex Incorporated)Wyomissing, PA, United StatesSpecification developer1October 17, 1996010api.fda.gov
Arrow International, LLC (subsidiary of Teleflex, Incorporated)Chelmsford, MA, United StatesManufacturer1October 17, 1996000api.fda.gov
Ethicon, Inc.Somerville, NJ, United StatesManufacturer1August 2, 2018000api.fda.gov
Ethicon, Inc.Raritan, NJ, United StatesSpecification developer1August 2, 2018000api.fda.gov
Ethicon, LLC.San Lorenzo, PR, United StatesManufacturer1August 2, 2018000api.fda.gov
Gamamed Vascular Systems Inc.Loveland, CO, United StatesManufacturer, Repackager or relabeler1June 15, 2025000api.fda.gov
C.R. Bard, Inc.Queensbury, NY, United StatesContract manufacturer0000api.fda.gov
Harmac Medical Products, Inc.Buffalo, NY, United StatesContract manufacturer0000api.fda.gov
Medtronic Perfusion SystemsMinneapolis, MN, United StatesSpecification developer0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesContract manufacturer0000api.fda.gov
Medtronic Grand RapidsGrand Rapids, MI, United StatesManufacturer0000api.fda.gov
Solo Pace IncBrooklyn Park, MN, United StatesSpecification developer0000api.fda.gov
Technical Services For Electronics, Inc.Jackson, MN, United StatesContract manufacturer0000api.fda.gov
TZ Medical, Inc.Tualatin, OR, United StatesContract manufacturer0000api.fda.gov
Vascular Solutions LLCMaple Grove, MN, United StatesManufacturer0000api.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.