Data / Medical devices / Subsystem, Water Purification

Subsystem, Water Purification (FIP): 48 FDA-registered makers in 7 countries

48 establishments in 7 countries are registered with the FDA to make Subsystem, Water Purification (product code FIP, Class 2, 21 CFR 876.5665). 25 of them have a 510(k) clearance or PMA approval on file and 4 have a recall event. The FDA has issued 117 510(k) clearances under this code, the latest on November 14, 2025, and lists 13 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code

FIP

Device class

2

Regulation

876.5665

Medical specialty

Gastroenterology, Urology

Makers by country

Makers of Subsystem, Water Purification

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.

Updated November 14, 2025. 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.