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Data / Medical devices / Catheter, Recording, Electrode, Reprocessed / United States

FDA-registered makers of Catheter, Recording, Electrode, Reprocessed in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Catheter, Recording, Electrode, Reprocessed (product code NLH). 5 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
Catheter, Recording, Electrode, Reprocessed
Product code
NLH
Country
United States

Makers of Catheter, Recording, Electrode, Reprocessed in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Innovative Health, LLC.Scottsdale, AZ, United StatesReprocessor21June 7, 2024000api.fda.gov
Stryker Sustainability Solutions PhoenixPhoenix, AZ, United StatesReprocessor17May 13, 2020010api.fda.gov
Stryker Sustainability SolutionsTempe, AZ, United StatesSpecification developer14May 13, 20200100api.fda.gov
Sterilmed, Inc.Plymouth, MN, United StatesReprocessor, Specification developer10October 11, 2024000api.fda.gov
Medline ReNewalRedmond, OR, United StatesReprocessor3November 26, 2025000api.fda.gov
Nypro Inc (Maple Grove)Maple Grove, MN, 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.