510(k) Report

510(k) · Cleared

Cleared

Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath (Diagnostic)

K192278510(k) SpecialCleared Nov 1, 201971-day reviewClass II21 CFR 884.1690

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

Uvision360, Inc. · HIH Hysteroscope (And Accessories)

Cleared on Nov 1, 2019 as substantially equivalent to K190827 (Uvision360, Inc., 2019) after a 71-day review. Its family tree reaches back 10 generations to 1992. 1 later device descends from it.

Decided
Nov 1, 2019
Review
71 days
Class
Class II
Product code
HIH
Recalls
None
Predicates
1

Its longest line of descent runs back 10 generations to K921244 (1992). 21 ancestors in all, the oldest K843084 (1985). 1 later device descends from it, 1 citing it directly.

  1. Root · 10 generations backK921244 Disposable Protective SheathVision-Sciences, Inc. · 1992
  2. 6 generations between
  3. 3 generations backK071127 Flexible Hysteroscope with Endosheath SystemVision-Sciences, Inc. · 2007
  4. 2 generations backK181909 Luminelle DTx Hysteroscopy SystemUvision360, Inc. · 2018
  5. 1 generation backK190827 Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile…Uvision360, Inc. · 2019
  6. This deviceK192278 Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable…Uvision360, Inc. · 2019
  7. Descendant · cites it directly · 0 of its ownK210512 LUMINELLE DTx SystemUvision360, Inc. · 2021
Show all 10 generations
  1. Root · 10 generations backK921244 Disposable Protective SheathVision-Sciences, Inc. · 1992
  2. 9 generations backK961591 Disposable Endosheath for E-F100 Flexible NasopharyngoscopeVision-Sciences, Inc. · 1996
  3. 8 generations backK963795 Vision-Sciences Model B-F100 Bronchoscope with Model BS-F21…Vision-Sciences, Inc. · 1996
  4. 7 generations backK021344 B-F200 Bronchoscope with BSS-F21 Endosheath SystemVision-Sciences, Inc. · 2002
  5. 6 generations backK031786 Tne-2000 Esophagoscope with Ecs-D Endosheath SystemVision-Sciences, Inc. · 2003
  6. 5 generations backK040215 Vision-Sciences CST-2000 Flexible Cystoscope with Slide-on…Vision-Sciences, Inc. · 2004
  7. 4 generations backK053560 Modified Endosheath System for Vsi Flexible CystoscopeVision-Sciences, Inc. · 2006
  8. 3 generations backK071127 Flexible Hysteroscope with Endosheath SystemVision-Sciences, Inc. · 2007
  9. 2 generations backK181909 Luminelle DTx Hysteroscopy SystemUvision360, Inc. · 2018
  10. 1 generation backK190827 Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile…Uvision360, Inc. · 2019
  11. This deviceK192278 Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable…Uvision360, Inc. · 2019

Most influential descendants

Showing 1 of 1 · See all
  • K210512LUMINELLE DTx SystemUvision360, Inc. · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K921244Disposable Protective SheathVision-Sciences, Inc.1992—
−9K961591Disposable Endosheath for E-F100 Flexible NasopharyngoscopeVision-Sciences, Inc.1996—
−8K963795Vision-Sciences Model B-F100 Bronchoscope with Model BS-F21 Disposable…Vision-Sciences, Inc.1996—
−7K021344B-F200 Bronchoscope with BSS-F21 Endosheath SystemVision-Sciences, Inc.2002—
−6K031786Tne-2000 Esophagoscope with Ecs-D Endosheath SystemVision-Sciences, Inc.2003—
−5K040215Vision-Sciences CST-2000 Flexible Cystoscope with Slide-on Endosheath SystemVision-Sciences, Inc.2004—
−4K053560Modified Endosheath System for Vsi Flexible CystoscopeVision-Sciences, Inc.2006—
−3K071127Flexible Hysteroscope with Endosheath SystemVision-Sciences, Inc.2007—
−2K181909Luminelle DTx Hysteroscopy SystemUvision360, Inc.2018—
−1K190827Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable…Uvision360, Inc.2019—
0 (this device)K192278Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable…Uvision360, Inc.2019—
+1K210512LUMINELLE DTx SystemUvision360, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198910
199220
199320
199410
199610
199910
200210
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
FIG. 1 — Lineage of K192278, 1992–2021Source: 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 HIH? 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 HIH device

  1. #1 K232003 Endoscopic Video Image Processor, Single-Use…score 16.1 · 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? (1)

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
*K190827Luminelle DTx Hysteroscopy System, Luminelle 360 Rotatable Sterile Disposable Sheath Rigid
Summary page 4
…oscope (and accessories); Cystoscope (and accessories) 510(k) Submitter / Holder UVision360 Inc. 510(k) Number K190827 Regulation Number 21 CFR 884.1690 Hysteroscope and accessories 21 CFR 876.1500 En…
Uvision360, Inc.2019—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K210512LUMINELLE DTx SystemUvision360, Inc.20210

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?

  • The line of descent spans 27 years and passes through 2 companies; a new generation was cleared every 1.7 years on median.
  • 3 of the 21 ancestors have a recall of any class.
  • Of its descendants, K210512 (Uvision360, Inc., 2021) has gone furthest, with 0 descendants of its own.

How does its category compare?

All HIH devices

HIH Hysteroscope (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · HIH

3in 2025

2007: 12008: 22009: 42010: 42011: 32012: 42013: 52014: 22015: 52016: 32017: 22018: 82019: 142020: 72021: 42022: 22023: 42024: 62025: 32026 (partial year): 7
2007high 14 (2019) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HIH

111in 2025

2009: 130 days median2010: 109 days median2011: 118 days median2012: 25 days median2013: 144 days median2015: 52 days median2016: 106 days median2018: 135 days median2019: 91 days median2020: 88 days median2021: 194 days median2023: 200 days median2024: 148 days median2025: 111 days median2026 (partial year): 168 days median
2007high 200 (2023) · low 25 (2012)2026

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

Recalls per year · HIH

3so far in 2026, the most since 2007

2019: 12023: 22026 (partial year): 3
2007high 3 (2026) · low 0 (2007)2026

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

Adverse event reports per year · HIH

1,698in 2025

2007: 72008: 122009: 172010: 312011: 592012: 782013: 1112014: 1252015: 2112016: 1722017: 3362018: 1822019: 2202020: 2532021: 1932022: 2892023: 1,4492024: 1,6112025: 1,698
2007high 1,698 (2025) · low 7 (2007)2025

MAUDE reports naming product code HIH, 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
20071—07
20082—012
20094130017
20104109031
20113118059
2012425078
201351440111
20142—0125
20155520211
201631060172
20172—0336
201881350182
201914911220
20207880253
202141940193
20222—0289
2023420021,449
2024614801,611
2025311101,698
202671683—

What is it indicated for?

Hysteroscopy: The LUMINELLE DTx Hysteroscopy System is used to permit viewing of the cervical canal and uterine cavity for the purpose of performing diagnostic and surgical procedures. NOTE: Hysteroscopes are used as tools to access the uterine cavity and are not, in and of themselves, a method of surgery. When LUMINELLE DTx Hysteroscopy System is specifically used with the LUMINELLE Dx 360 Rotatable Disposable Sheath (Diagnostic), the system is limited…

Read the full statement (203 words)

Hysteroscopy: The LUMINELLE DTx Hysteroscopy System is used to permit viewing of the cervical canal and uterine cavity for the purpose of performing diagnostic and surgical procedures.

NOTE: Hysteroscopes are used as tools to access the uterine cavity and are not, in and of themselves, a method of surgery. When LUMINELLE DTx Hysteroscopy System is specifically used with the LUMINELLE Dx 360 Rotatable Disposable Sheath (Diagnostic), the system is limited to performing diagnostic procedures only.

Generally recognized indications for diagnostic hysteroscopy include:

• Abnormal bleeding

• Infertility and pregnancy wastage

• Evaluation of abnormal hysterosalpingogram

• Intrauterine foreign body

• Amenorrhea

• Pelvic Pain

Generally recognized indications for use for operative hysteroscopy include:

• Directed endometrial biopsy

• Polypectomy

• Submucous myomectomy

• Transection of intrauterine adhesions

• Transection of intrauterine septa

• Endometrial ablation

Cystoscopy: The LUMINELLE DTx Hysteroscopy System is intended for use in endoscopic access to and examination of the lower urinary tract, including the bladder. When combined with accessory instruments, the System allows the user to perform various diagnostic and therapeutic procedures.

NOTE: When LUMINELLE DTx Hysteroscopy System is specifically used with the LUMINELLE Dx 360 Rotatable Disposable Sheath (Diagnostic), the system is limited to performing diagnostic procedures only.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K192278: Luminelle DTx Hysteroscopy System, Luminelle Dx 360 Rotatable Disposable Sheath (Diagnostic).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K192278

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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