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Data / Medical devices / Pacemaker Lead Adaptor / United States

FDA-registered makers of Pacemaker Lead Adaptor in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Pacemaker Lead Adaptor (product code DTD). 6 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Pacemaker Lead Adaptor
Product code
DTD
Country
United States

Makers of Pacemaker Lead Adaptor in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Oscor Inc.Palm Harbor, FL, United StatesComplaint file establishment, Manufacturer5March 19, 2015000api.fda.gov
Medtronic, Inc.Mounds View, MN, United StatesManufacturer, Specification developer3February 23, 2000000api.fda.gov
Abbott MedicalSylmar, CA, United StatesManufacturer2April 6, 1995000api.fda.gov
Medtronic Puerto Rico Operations Co., VillalbaVillalba, PR, United StatesManufacturer2April 18, 1991000api.fda.gov
Boston Scientific CorporationSaint Paul, MN, United StatesComplaint file establishment, Manufacturer, Specification developer1September 20, 1984000api.fda.gov
Greatbatch MedicalMinneapolis, MN, United StatesManufacturer1March 3, 1987000api.fda.gov
Heraeus Medical Components Caribe, Inc.Dorado, PR, United StatesContract manufacturer0000api.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.