510(k) Report

510(k) · Cleared

Cleared

Flexible Nasopharyngo-Laryngoscope and Endosheath

K942265510(k) TraditionalCleared Dec 22, 1995592-day reviewClass II21 CFR 874.4760

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

Vision-Sciences, Inc. · EOB Nasopharyngoscope (Flexible Or Rigid)

Cleared on Dec 22, 1995 after a 592-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 32 later devices descend from it.

Decided
Dec 22, 1995
Review
592 days
Class
Class II
Product code
EOB
Recalls
None
Predicates
0

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

Descendants, by year cleared 2004: 1 descendant cleared2007: 1 descendant cleared2005: 1 descendant cleared2008: 1 descendant cleared2010: 1 descendant cleared2017: 2 descendants cleared2011: 3 descendants cleared2012: 2 descendants cleared2009: 2 descendants cleared2015: 4 descendants cleared2014: 4 descendants cleared2013: 1 descendant cleared2018: 1 descendant cleared2020: 2 descendants cleared2021: 1 descendant cleared2022: 2 descendants cleared2016: 1 descendant cleared2023: 2 descendants cleared1995200020052010201520202025
  1. This deviceK942265 Flexible Nasopharyngo-Laryngoscope and EndosheathVision-Sciences, Inc. · 1995
  2. Descendant · cites it directly · 30 of its ownK050972 Vision-Sciences Ent-3000 ScopeVision-Sciences, Inc. · 2005 · Recalled
  3. Descendant · cites it directly · 30 of its ownK040984 Vision Sciences Model Ent-2000V Flexible Nasopharyngo-LaryngoscopeVision-Sciences, Inc. · 2004
  4. Descendant · cites it directly · 29 of its ownK072073 Vision-Sciences Ent-5000 and Ent-5100 Video Ent Scope with…Vision-Sciences, Inc. · 2007
  5. Descendant · cites it directly · 15 of its ownK080622 Entity Nasoview Led Nasopharyngoscope, Model 006105Optim, Inc. · 2008
  6. Descendant · 2 generations on · 9 of its ownK091829 PLS Portable Light SourceOptim, Inc. · 2009

Showing 5 of 32 descendants. See all descendants

Descendants cleared per year

2004: 12005: 12007: 12008: 12009: 22010: 12011: 32012: 22013: 12014: 42015: 42016: 12017: 22018: 12020: 22021: 12022: 22023: 2
2004high 4 (2014) · low 0 (2006)2026

Most influential descendants

Showing 5 of 32 · See all
  • K050972Vision-Sciences Ent-3000 ScopeVision-Sciences, Inc. · 2005 · cites it directly30descendants
  • K040984Vision Sciences Model Ent-2000V Flexible Nasopharyngo-LaryngoscopeVision-Sciences, Inc. · 2004 · cites it directly30descendants
  • K072073Vision-Sciences Ent-5000 and Ent-5100 Video Ent Scope with Endosheath System…Vision-Sciences, Inc. · 2007 · cites it directly29descendants
  • K080622Entity Nasoview Led Nasopharyngoscope, Model 006105Optim, Inc. · 2008 · cites it directly15descendants
  • K091829PLS Portable Light SourceOptim, Inc. · 2009 · 2 generations on9descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K942265Flexible Nasopharyngo-Laryngoscope and EndosheathVision-Sciences, Inc.1995—
+1K050972Vision-Sciences Ent-3000 ScopeVision-Sciences, Inc.20052
+1K040984Vision Sciences Model Ent-2000V Flexible Nasopharyngo-LaryngoscopeVision-Sciences, Inc.2004—
+1K072073Vision-Sciences Ent-5000 and Ent-5100 Video Ent Scope with Endosheath System…Vision-Sciences, Inc.2007—
+1K080622Entity Nasoview Led Nasopharyngoscope, Model 006105Optim, Inc.2008—
+2K091829PLS Portable Light SourceOptim, Inc.2009—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200510
200710
200810
200920
201010
201130
201220
201310
201440
201540
201610
201720
201810
202020
202110
202220
202320
FIG. 1 — Lineage of K942265, 1995–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 EOB? 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 EOB device

  1. #1 K253184 Video Rhinolaryngoscope System (Disposable…score 14.4 · 12 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (32)

See all 32

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K050972Vision-Sciences Ent-3000 ScopeVision-Sciences, Inc.200530
K040984Vision Sciences Model Ent-2000V Flexible Nasopharyngo-LaryngoscopeVision-Sciences, Inc.200430
K072073Vision-Sciences Ent-5000 and Ent-5100 Video Ent Scope with Endosheath System…Vision-Sciences, Inc.200729
K080622Entity Nasoview Led Nasopharyngoscope, Model 006105Optim, Inc.200815

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, K050972 (Vision-Sciences, Inc., 2005) has gone furthest, with 30 descendants of its own.

How does its category compare?

All EOB devices

EOB Nasopharyngoscope (Flexible Or Rigid): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EOB

3in 2025

2007: 42008: 42009: 12010: 12011: 42012: 12014: 32015: 32016: 32017: 62018: 62019: 82020: 32021: 22022: 62023: 32024: 22025: 32026 (partial year): 5
2007high 8 (2019) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EOB

192in 2025

2007: 37 days median2008: 38 days median2011: 209 days median2014: 282 days median2015: 115 days median2016: 174 days median2017: 216 days median2018: 230 days median2019: 149 days median2020: 175 days median2022: 178 days median2023: 107 days median2025: 192 days median2026 (partial year): 180 days median
2007high 282 (2014) · low 37 (2007)2026

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

Recalls per year · EOB

1in 2023

2011: 22022: 12023: 12026 (partial year): 1
2007high 2 (2011) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EOB

1,338in 2025

2007: 12008: 12009: 32011: 32012: 42013: 52014: 52015: 132016: 162017: 182018: 232019: 512020: 472021: 3452022: 1,1582023: 1,3522024: 1,4982025: 1,338
2007high 1,498 (2024) · low 0 (2010)2025

MAUDE reports naming product code EOB, 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
200743701
200843801
20091—03
20101—00
2011420923
20121—04
20130—05
2014328205
20153115013
20163174016
20176216018
20186230023
20198149051
20203175047
20212—0345
2022617811,158
2023310711,352
20242—01,498
2025319201,338
202651801—
Cite this page

510(k) Report. “K942265: Flexible Nasopharyngo-Laryngoscope and Endosheath.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K942265

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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