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
| Country | Makers |
|---|---|
| United States | 3 |
| France | 2 |
| Italy | 2 |
| United Kingdom | 1 |
| Switzerland | 1 |
| Germany | 1 |
| Taiwan | 1 |
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.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Nephros, Inc. | South Orange, NJ, United States | Complaint file establishment, Specification developer | 3 | December 22, 2016 | 0 | 0 | 0 | api.fda.gov |
| Global Life Sciences Solutions USA LLC | Marlborough, MA, United States | Complaint file establishment, Specification developer | 2 | June 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Pall Newquay | Newquay Cornwall, United Kingdom | Manufacturer | 2 | June 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Pall International, Sarl | Fribourg, Switzerland | Exporter to the US, Specification developer | 2 | June 1, 2017 | 0 | 0 | 0 | api.fda.gov |
| Aqua-Tools | Paris Yvelines, France | Complaint file establishment, Specification developer | 1 | October 25, 2019 | 0 | 0 | 0 | api.fda.gov |
| CS Medical LLC | Creedmoor, NC, United States | Specification developer | 1 | October 24, 2014 | 0 | 0 | 0 | api.fda.gov |
| i3 Membrane GmbH | Radeberg Saxony, Germany | Complaint file establishment, Manufacturer | 1 | June 2, 2023 | 0 | 0 | 0 | api.fda.gov |
| Caware Filtering Corporation | Kaohsiung, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Infiplast | OYONNAX Ain, France | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medica S.p.A. | Medolla Modena, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sarmed SRL | IGLESIAS Sardegna, Italy | Contract manufacturer | 0 | 0 | 0 | 0 | api.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.