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Data / Medical devices / System, Water Purification, General Medical Use

System, Water Purification, General Medical Use (NHV): 11 FDA-registered makers in 7 countries

11 establishments in 7 countries are registered with the FDA to make System, Water Purification, General Medical Use (product code NHV, Class 2, 21 CFR 876.5665). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 12 510(k) clearances under this code, the latest on September 9, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
NHV
Device class
2
Regulation
876.5665
Medical specialty
Gastroenterology, Urology

Makers by country

CountryMakers
United States3
France2
Italy2
United Kingdom1
Switzerland1
Germany1
Taiwan1

Makers of System, Water Purification, General Medical Use

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Nephros, Inc.South Orange, NJ, United StatesComplaint file establishment, Specification developer3December 22, 2016000api.fda.gov
Global Life Sciences Solutions USA LLCMarlborough, MA, United StatesComplaint file establishment, Specification developer2June 1, 2017000api.fda.gov
Pall NewquayNewquay Cornwall, United KingdomManufacturer2June 1, 2017000api.fda.gov
Pall International, SarlFribourg, SwitzerlandExporter to the US, Specification developer2June 1, 2017000api.fda.gov
Aqua-ToolsParis Yvelines, FranceComplaint file establishment, Specification developer1October 25, 2019000api.fda.gov
CS Medical LLCCreedmoor, NC, United StatesSpecification developer1October 24, 2014000api.fda.gov
i3 Membrane GmbHRadeberg Saxony, GermanyComplaint file establishment, Manufacturer1June 2, 2023000api.fda.gov
Caware Filtering CorporationKaohsiung, TaiwanContract manufacturer0000api.fda.gov
InfiplastOYONNAX Ain, FranceContract manufacturer0000api.fda.gov
Medica S.p.A.Medolla Modena, ItalyContract manufacturer0000api.fda.gov
Sarmed SRLIGLESIAS Sardegna, ItalyContract manufacturer0000api.fda.gov

Updated September 9, 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.