510(k) Report

510(k) · Decided

Recalled · Class II · 2026

Mic Peg Tube

K924065510(k) TraditionalDecided Feb 17, 1994570-day reviewClass II21 CFR 876.5980Recalls 14

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

Medical Innovations Corp. · KNT Tubes, Gastrointestinal (And Accessories)

Cleared on Feb 17, 1994 after a 570-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it. It has been recalled 14 times.

Decided
Feb 17, 1994
Review
570 days
Class
Class II
Product code
KNT
Recalls
14
Predicates
0

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

Descendants, by year cleared 2006: 1 descendant cleared2018: 1 descendant cleared1990200020102020
  1. This deviceK924065 Mic Peg TubeMedical Innovations Corp. · 1994
  2. Descendant · cites it directly · 1 of its ownK061021 Entake Standard and Safety Peg SystemConmedcorp · 2006 · Recalled
  3. Descendant · 2 generations on · 0 of its ownK182248 Aspire Venting TubeAspire Bariatrics, Inc. · 2018

Most influential descendants

Showing 2 of 2 · See all
  • K061021Entake Standard and Safety Peg SystemConmedcorp · 2006 · cites it directly1descendant
  • K182248Aspire Venting TubeAspire Bariatrics, Inc. · 2018 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K924065Mic Peg TubeMedical Innovations Corp.1994—
+1K061021Entake Standard and Safety Peg SystemConmedcorp200628
+2K182248Aspire Venting TubeAspire Bariatrics, Inc.2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
201810
FIG. 1 — Lineage of K924065, 1994–2018Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K061021Entake Standard and Safety Peg SystemConmedcorp20061

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

Recalls of this device

DateClassRecallRoot causeReason
Apr 30, 2026Class IIZ-2344-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2349-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2350-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2348-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2341-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2342-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2352-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2347-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2345-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2351-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2346-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Apr 30, 2026Class IIZ-2343-2026Material/Component ContaminationLidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Dec 22, 2021Class IIZ-0565-2022Under Investigation by firmThe External Retention Bolster contained in the kit may be a larger diameter than the tube.
Dec 22, 2021Class IIZ-0566-2022Under Investigation by firmThe External Retention Bolster contained in the kit may be a larger diameter than the tube.

The 5 latest of 14 recalls; the web page lists all.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K061021 (Conmedcorp, 2006) has gone furthest, with 1 descendant 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.

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—

More from Medical Innovations Corp.

24 FDA decisions under this applicant name. See the company

  • K945612Mic Nasogastric-Gastrojejunal Feeding TubeMedical Innovations Corp. · 1995
  • K940548Mic Percutaneous Endoscopic Jejunal Feeding TubeMedical Innovations Corp. · 1995
  • K943685Mic Disposable SnareMedical Innovations Corp. · 1994
  • K926581Mic Transgastric Jejunal TubeMedical Innovations Corp. · 1994
  • K921370Mic Gastro-Enterostomy Tube ModificationMedical Innovations Corp. · 19942 Class I recalls

Recent decisions in KNT

The KNT category page

  • K262038danumed StomaMeterDanumed Medizintechnik GmbH · 2026
  • K26189052Fr ViSiGi LUX™; 52Fr ViSiGi 3D®Boehringer Laboratories, LLC · 2026
  • K253514Minnesota Four-Lumen Esophagogastric Tamponade Tube - 18 French (0092220); Blakemore Esophageal-Nasogastric…C.R. Bard, Inc. · 2026
  • K250389XNY Disposable Gastric Calibration TubeChangzhou Xin Neng Yuan Medical Stapler Co.,Ltd · 2025
  • K243228Flexi-Seal AIR (with ENFit Connector)Convatec · 2025

https://510kreport.com/device/K924065 · printed Nov 5, 2026

Cite this page

510(k) Report. “K924065: Mic Peg Tube.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K924065

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026