510(k) · Cleared
Recalled · Class II · 2024AquaC UNO H
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Vivonic GmbH · FIP Subsystem, Water Purification
Cleared on Oct 19, 2015 as substantially equivalent to K110578 (Mar Cor Purification, Inc., 2011) and 1 other predicate after a 304-day review. Its family tree reaches back 4 generations to 1981. 1 later device descends from it. It has been recalled 5 times.
- Decided
- Oct 19, 2015
- Review
- 304 days
- Class
- Class II
- Product code
- FIP
- Recalls
- 5
- Predicates
- 2
Its longest line of descent runs back 4 generations to K811678 (1981). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 4 generations backK811678 Gambro Water Purification Monitor WRDGambro, Inc. · 1981
- 3 generations backK042797 Wro 300 Water Purification System for HemodialysisGambro Renal Products · 2005
- 2 generations backK093608 Gambro Water Purification Unit, Models Wro 300 and Wro 300 HGambro Renal Products, Inc. · 2010
- 1 generation backK110578 Millenium HX Portable Reverse Osmosis Water Purification SystemMar Cor Purification, Inc. · 2011 · Recalled
- This deviceK143617 AquaC UNO HVivonic GmbH · 2015
- Descendant · cites it directly · 0 of its ownK250471 AquaC UNO HFresenius Medical Care Renal Therapies Group, LLC · 2025
Most influential descendants
Showing 1 of 1 · See all- K250471AquaC UNO HFresenius Medical Care Renal Therapies Group, LLC · 2025 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K811678 | Gambro Water Purification Monitor WRD | Gambro, Inc. | 1981 | — |
| −3 | K042797 | Wro 300 Water Purification System for Hemodialysis | Gambro Renal Products | 2005 | — |
| −2 | K093608 | Gambro Water Purification Unit, Models Wro 300 and Wro 300 H | Gambro Renal Products, Inc. | 2010 | — |
| −1 | K110578 | Millenium HX Portable Reverse Osmosis Water Purification System | Mar Cor Purification, Inc. | 2011 | 1 |
| 0 (this device) | K143617 | AquaC UNO H | Vivonic GmbH | 2015 | — |
| +1 | K250471 | AquaC UNO H | Fresenius Medical Care Renal Therapies Group, LLC | 2025 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1997 | 1 | 0 |
| 2001 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2025 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FIP? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new FIP device
- #1 K251851 DIASAFEplusUS (F00013010)score 14.0 · 14 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K110578 | Millenium HX Portable Reverse Osmosis Water Purification SystemSummary page 5…Page 2 of 4 Claiming substantial equivalence to K110578 Mar Cor Millenium HX K093608 Mar Cor WRO 300 H Device Description The AquaC UNO H Water Pur… | 2011 |
| * | K093608 | Gambro Water Purification Unit, Models Wro 300 and Wro 300 HSummary page 5…Page 2 of 4 Claiming substantial equivalence to K110578 Mar Cor Millenium HX K093608 Mar Cor WRO 300 H Device Description The AquaC UNO H Water Purification System is a microcontroller-controll… | 2010 |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K250471 | AquaC UNO H | 2025 | 0 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| May 16, 2024 | Class II | Z-2141-2024 | Process control | Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard default set point range is between 4 and 18.Error message (F020104, "concentrate pressure alarm limit exceeded") concentrate pressure is too high and stops the… |
| Jun 21, 2022 | Class II | Z-1769-2022 | Under Investigation by firm | Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured |
| Jun 21, 2022 | Class II | Z-1770-2022 | Under Investigation by firm | Internal ethemet cables are missing one or both ferrite cores therefore the electromagnetic compatibility of the device is not ensured |
| Jun 16, 2022 | Class II | Z-1463-2022 | Under Investigation by firm | Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the… |
| Jun 16, 2022 | Class II | Z-1464-2022 | Under Investigation by firm | Internal ethernet cable may be misaligned, the cable jacket (insulation) could become compromised due to high temperature and result in the internal ethernet cable conducting electrical current to the ethernet port on the outside of the… |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 34 years and passes through 5 companies; a new generation was cleared every 5.4 years on median.
- 1 of the 6 ancestors has a recall of any class.
- Of its descendants, K250471 (Fresenius Medical Care Renal Therapies Group, LLC, 2025) has gone furthest, with 0 descendants of its own.
- 3 other devices also cite its predicate K110578.
How does its category compare?
All FIP devicesFIP Subsystem, Water Purification: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · FIP
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FIP
88in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FIP
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FIP
77in 2025
MAUDE reports naming product code FIP, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 0 | 1 |
| 2008 | 3 | 202 | 0 | 5 |
| 2009 | 3 | 167 | 0 | 0 |
| 2010 | 2 | — | 0 | 12 |
| 2011 | 4 | 116 | 0 | 4 |
| 2012 | 2 | — | 0 | 4 |
| 2013 | 4 | 125 | 0 | 41 |
| 2014 | 4 | 126 | 0 | 34 |
| 2015 | 2 | — | 0 | 12 |
| 2016 | 2 | — | 0 | 3 |
| 2017 | 1 | — | 0 | 6 |
| 2018 | 1 | — | 0 | 3 |
| 2019 | 2 | — | 0 | 13 |
| 2020 | 1 | — | 1 | 12 |
| 2021 | 1 | — | 0 | 35 |
| 2022 | 1 | — | 0 | 57 |
| 2023 | 3 | 69 | 0 | 140 |
| 2024 | 1 | — | 0 | 174 |
| 2025 | 4 | 88 | 0 | 77 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The AquaC UNO H Portable Water Purification System is a reverse osmosis unit intended for use with hemodialysis systems to remove organic and inorganic substances and microbial contaminants from the water used for treating hemodialysis patients or related therapies.
The AquaC UNO H can be connected to hemodialysis equipment used in hospitals, clinics and in home environments. This device is intended to be a component in a complete water purification system, and is not a complete water treatment system. The reverse osmosis unit must be preceded by pre-treatment devices, and may need to be followed by post-treatment devices as well, to meet current AAMI/ANSI and FDA recognized U.S. standards.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K143617 · printed Nov 6, 2026
Cite this page
510(k) Report. “K143617: AquaC UNO H.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K143617
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026