510(k) Report

510(k) · Cleared

Cleared

Metrixcare

K132424510(k) TraditionalCleared Feb 12, 2014191-day reviewClass II21 CFR 876.5980

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

The Metrix Company · KNT Tubes, Gastrointestinal (And Accessories)

Cleared on Feb 12, 2014 after a 191-day review. The FDA summary names its predicate without a number. 4 later devices descend from it.

Decided
Feb 12, 2014
Review
191 days
Class
Class II
Product code
KNT
Recalls
None
Predicates
0

4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2017: 1 descendant cleared2019: 1 descendant cleared2023: 1 descendant cleared2025: 1 descendant cleared2010201520202025
  1. This deviceK132424 MetrixcareThe Metrix Company · 2014
  2. Descendant · cites it directly · 3 of its ownK170555 U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC · 2017
  3. Descendant · 2 generations on · 2 of its ownK190310 U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC · 2019
  4. Descendant · 3 generations on · 0 of its ownK242917 Enteral Drainage System, Enteral Medicine strawHMC Premedical S.p.A. · 2025
  5. Descendant · 3 generations on · 0 of its ownK223683 EnteraLoc FlowVonco Products · 2023

Most influential descendants

Showing 4 of 4 · See all
  • K170555U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC · 2017 · cites it directly3descendants
  • K190310U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC · 2019 · 2 generations on2descendants
  • K242917Enteral Drainage System, Enteral Medicine strawHMC Premedical S.p.A. · 2025 · 3 generations on0descendants
  • K223683EnteraLoc FlowVonco Products · 2023 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K132424MetrixcareThe Metrix Company2014—
+1K170555U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC2017—
+2K190310U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC2019—
+3K242917Enteral Drainage System, Enteral Medicine strawHMC Premedical S.p.A.2025—
+3K223683EnteraLoc FlowVonco Products2023—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201910
202310
202510
FIG. 1 — Lineage of K132424, 2014–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 KNT? 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 KNT device

  1. #1 K261890 52Fr ViSiGi LUX™; 52Fr ViSiGi 3D®score 12.7 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (5)

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.

TypeNumberDeviceApplicantDecidedRecalls
*—500 ml Enteral Bag with Gravity Set (Predicate Model 51584)
Named without a submission number
—
*—1000 ml Enteral Bag with Gravity Set (Predicate Model as listed in the comparison table)
Named without a submission number
—
*—1000 ml Enteral Bag with Screw Cap & Gravity Set (Predicate Model 0009)
Named without a submission number
—
*—Gravity Set with Feeding Cap (Predicate Model 0061)
Named without a submission number
—
*—Gravity Set with Cross Screw Connector (Predicate Model 62552)
Named without a submission number
—

What descends from it? (4)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K170555U Deliver Bolink ENFit Enteral Feeding SetsU Deliver Medical, LLC20173

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K170555 (U Deliver Medical, LLC, 2017) has gone furthest, with 3 descendants of its own.

How does its category compare?

All KNT devices

KNT Tubes, Gastrointestinal (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · KNT

4in 2025

2007: 102008: 102009: 112010: 122011: 72012: 122013: 72014: 162015: 102016: 62017: 92018: 72019: 102020: 52021: 62022: 72023: 52024: 92025: 42026 (partial year): 3
2007high 16 (2014) · low 4 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KNT

136in 2025

2007: 118 days median2008: 115 days median2009: 102 days median2010: 104 days median2011: 211 days median2012: 107 days median2013: 128 days median2014: 259 days median2015: 140 days median2016: 99 days median2017: 247 days median2018: 149 days median2019: 126 days median2020: 102 days median2021: 121 days median2022: 110 days median2023: 162 days median2024: 103 days median2025: 136 days median2026 (partial year): 105 days median
2007high 259 (2014) · low 99 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · KNT

13in 2025

2007: 12008: 822009: 92010: 32011: 22012: 12015: 12016: 32017: 42018: 22019: 22020: 12021: 22022: 1, 1 Class I2023: 22025: 132026 (partial year): 20
2007high 82 (2008) · low 0 (2013)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · KNT

1,451in 2025

2007: 3002008: 8672009: 8182010: 5172011: 5312012: 5282013: 7472014: 1,0302015: 1,0482016: 1,2512017: 1,6722018: 1,9012019: 1,8382020: 1,6412021: 1,6552022: 1,6502023: 1,8632024: 1,3442025: 1,451
2007high 1,901 (2018) · low 300 (2007)2025

MAUDE reports naming product code KNT, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007101181300
20081011582867
2009111029818
2010121043517
201172112531
2012121071528
201371280747
20141625901,030
20151014011,048
201669931,251
2017924741,672
2018714921,901
20191012621,838
2020510211,641
2021612121,655
202271101 (1)1,650
2023516221,863
2024910301,344
20254136131,451
2026310520—

What is it indicated for?

The device is intended to deliver liquid nutritional formulas or water to a patient's enteral access device (feeding tube).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K132424: Metrixcare.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K132424

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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