510(k) Report

510(k) · Cleared

Cleared

Lungpoint Virtual Bronchoscopic Navigation VBN System

K090095510(k) TraditionalCleared Mar 13, 200957-day reviewClass II21 CFR 892.2050

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

Broncus Technologies, Inc. · LLZ System, Image Processing, Radiological

Cleared on Mar 13, 2009 as substantially equivalent to K080271 (Superdimension, Ltd., 2008) and 1 other predicate after a 57-day review. Its family tree reaches back 9 generations to 1993. 1 of the 25 devices in its family, counting itself, has a Class I recall. 7 later devices descend from it.

Decided
Mar 13, 2009
Review
57 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
2

Its longest line of descent runs back 9 generations to K926514 (1993). 17 ancestors in all, the oldest K882061 (1988). 7 later devices descend from it, 2 citing it directly. 1 of the 25 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2003: 1 other ancestor, 1 with a Class I recall12002: 1 other ancestor2000: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestor1991: 1 other ancestor1988: 1 other ancestor1993: 1 other ancestor2009: 2 descendants cleared2026: 1 descendant cleared2011: 1 descendant cleared2014: 1 descendant cleared2018: 1 descendant cleared2020: 1 descendant clearedK926514 · Endoscopic Ultrasound System Type 20 · Olympus Corp. · 1993 · recalledK951994 · Olympus EU-M30 Endoscopic Ultrasound Center · Olympus America, Inc. · 1996K982323 · Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary Equipment, for Bronchial Use · Olympus America, Inc. · 1998K042438 · Superdimension/Bronchus · Superdimension, Ltd. · 2004 · recalled×2: 2 generations cleared close together, K052260 (2005), K052852 (2005) K062315 · Superdimension/Bronchus Premium 2 · Superdimension, Ltd. · 2006 · recalledK071473 · Modification to Superdimension/Bronchus Premium 2 · Superdimension, Ltd. · 2007K080271 · Inreach System · Superdimension, Ltd. · 20081990200020102020
  1. Root · 9 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 5 generations between
  3. 3 generations backK062315 Superdimension/Bronchus Premium 2Superdimension, Ltd. · 2006 · Recalled
  4. 2 generations backK071473 Modification to Superdimension/Bronchus Premium 2Superdimension, Ltd. · 2007
  5. 1 generation backK080271 Inreach SystemSuperdimension, Ltd. · 2008
  6. This deviceK090095 Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc. · 2009
  7. Descendant · cites it directly · 5 of its ownK091160 Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc. · 2009
  8. Descendant · 2 generations on · 3 of its ownK112051 Lungpoint Planning and Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Technologies, Inc. · 2011
  9. Descendant · 3 generations on · 1 of its ownK181892 Ziostation2Ziosoft, Inc. · 2018
  10. Descendant · 2 generations on · 1 of its ownK093423 Lungpoint Procedure PlanningBroncus Technologies, Inc. · 2009
  11. Descendant · cites it directly · 0 of its ownK260009 LungPoint Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Medical, Inc. · 2026
Show all 9 generations
  1. Root · 9 generations backK926514 Endoscopic Ultrasound System Type 20Olympus Corp. · 1993 · Recalled
  2. 8 generations backK951994 Olympus EU-M30 Endoscopic Ultrasound CenterOlympus America, Inc. · 1996
  3. 7 generations backK982323 Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary…Olympus America, Inc. · 1998
  4. 6 generations backK042438 Superdimension/BronchusSuperdimension, Ltd. · 2004 · Recalled
  5. 5 generations backK052260 Superdimension/Bronchus 4.1Superdimension, Ltd. · 2005 · Recalled
  6. 4 generations backK052852 Superdimension/Bronchus PremiumSuperdimension, Ltd. · 2005 · Recalled
  7. 3 generations backK062315 Superdimension/Bronchus Premium 2Superdimension, Ltd. · 2006 · Recalled
  8. 2 generations backK071473 Modification to Superdimension/Bronchus Premium 2Superdimension, Ltd. · 2007
  9. 1 generation backK080271 Inreach SystemSuperdimension, Ltd. · 2008
  10. This deviceK090095 Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc. · 2009

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2009: 22011: 12014: 12018: 12020: 12026: 1
2009high 2 (2009) · low 0 (2010)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 7 · See all
  • K091160Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc. · 2009 · cites it directly5descendants
  • K112051Lungpoint Planning and Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Technologies, Inc. · 2011 · 2 generations on3descendants
  • K181892Ziostation2Ziosoft, Inc. · 2018 · 3 generations on1descendant
  • K093423Lungpoint Procedure PlanningBroncus Technologies, Inc. · 2009 · 2 generations on1descendant
  • K260009LungPoint Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Medical, Inc. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K926514Endoscopic Ultrasound System Type 20Olympus Corp.19931
−8K951994Olympus EU-M30 Endoscopic Ultrasound CenterOlympus America, Inc.1996—
−7K982323Olympus UM 2R/3R Ultrasonic Probes and Associated Ancillary Equipment, for…Olympus America, Inc.1998—
−6K042438Superdimension/BronchusSuperdimension, Ltd.20041
−5K052260Superdimension/Bronchus 4.1Superdimension, Ltd.20052
−4K052852Superdimension/Bronchus PremiumSuperdimension, Ltd.20051
−3K062315Superdimension/Bronchus Premium 2Superdimension, Ltd.20061
−2K071473Modification to Superdimension/Bronchus Premium 2Superdimension, Ltd.2007—
−1K080271Inreach SystemSuperdimension, Ltd.2008—
0 (this device)K090095Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc.2009—
+1K091160Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc.2009—
+2K112051Lungpoint Planning and Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Technologies, Inc.2011—
+3K181892Ziostation2Ziosoft, Inc.2018—
+2K093423Lungpoint Procedure PlanningBroncus Technologies, Inc.2009—
+1K260009LungPoint Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Medical, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199110
199310
199510
199610
200010
200210
200311

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200920
201110
201410
201810
202010
202610
FIG. 1 — Lineage of K090095, 1993–2026Source: 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.

1 device in this family has a Class I recall. 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K080271Inreach System
Summary page 1
…duct Code LLZ 4. Predicate Device The predicate device identified for the LungPoint VBN is as follows: superDimension®/Bronchus superDimension, Ltd K080271, cleared on inReach TM System March 31, 2008 superDimension/Bronchus…
Superdimension, Ltd.2008—
*K042438Superdimension/Bronchus
Summary page 1
…080271, cleared on inReach TM System March 31, 2008 superDimension/Bronchus superDimension, Ltd K042438, cleared on November 8, 2004 5. Device Description Thi…
Superdimension, Ltd.20041

Also cleared against K080271: 2 other devices →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K091160Lungpoint Virtual Bronchoscopic Navigation VBN SystemBroncus Technologies, Inc.20095
K260009LungPoint Virtual Bronchoscopic Navigation (VBN) SoftwareBroncus Medical, Inc.20260

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K023984Modification to Olympus Bronchoscopes BF-40 Series, BF-240 Series, and BF-160 SeriesThe Olympus Optical Co. · 2003 · 2 generations back · ◆ in the 2003 ancestors bar of FIG. 114 Class I recalls

What does this lineage say?

  • The line of descent spans 16 years and passes through 4 companies; a new generation was cleared every 10 months on median.
  • 8 of the 17 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K091160 (Broncus Technologies, Inc., 2009) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K080271.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

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

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

Indicated for displaying images of the tracheobronchial tree to aid the physician in guiding endoscopic tools or catheters in the pulmonary tract and to enable marker placement within soft lung tissue. It does not make a diagnosis and is not an endoscopic tool. Not for pediatric use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K090095: Lungpoint Virtual Bronchoscopic Navigation VBN System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K090095

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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