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Data / Medical devices / Dialyzer Reprocessing System / United States

FDA-registered makers of Dialyzer Reprocessing System in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Dialyzer Reprocessing System (product code LIF). 5 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
Dialyzer Reprocessing System
Product code
LIF
Country
United States

Makers of Dialyzer Reprocessing System in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Evoqua Water Technologies LLCMinneapolis, MN, United StatesManufacturer2November 27, 1990000api.fda.gov
Reprocessing Products Corporation (RPC)Tucson, AZ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer2February 10, 1999000api.fda.gov
Serim Research Corp.Elkhart, IN, United StatesManufacturer2April 9, 1992000api.fda.gov
Molded Products Inc.Harlan, IA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler1February 3, 2005000api.fda.gov
Novaflux, Inc.Princeton, NJ, United StatesManufacturer1November 3, 2010000api.fda.gov
IBT ScientificCreedmoor, NC, 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.