510(k) Report

510(k) · Cleared

Cleared

V-Raser Diode Laser System

K073332510(k) TraditionalCleared Feb 14, 200879-day reviewClass II21 CFR 878.4810

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

Hoya Conbio, Inc. · GEX Powered Laser Surgical Instrument

Cleared on Feb 14, 2008 as substantially equivalent to K063384 (Hoya Conbio, Inc., 2007) and 1 other predicate after a 79-day review. Its family tree reaches back 6 generations to 1992.

Decided
Feb 14, 2008
Review
79 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K922901 (1992). 26 ancestors in all, the oldest K883541 (1988). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2004: 1 other ancestor2005: 1 other ancestor2003: 1 other ancestor2001: 1 other ancestor1999: 1 other ancestor1998: 4 other ancestors1997: 3 other ancestors1995: 3 other ancestors1996: 2 other ancestors1990: 1 other ancestor1988: 1 other ancestor1994: 1 other ancestorK922901 · Incisor I Pulsed ND:Yag Laser System · Buckman Co., Inc. · 1992K972325 · Pulsemaster 1000 ST Dental Laser System · American Dental Technologies, Inc. · 1997K983058 · Ceralas D Laser System, Model # Ceralas D15 · Ceram Optec, Inc. · 1998K991891 · Ceralas Diode Laser System, Model Ceralas D15 · Ceram Optec, Inc. · 1999K053161 · Sirolaser · Sirona Dental Systems GmbH · 2006K063384 · Diodent Micro Dental Laser System, Models 810 and 980 · Hoya Conbio, Inc. · 2007198519901995200020052010
  1. Root · 6 generations backK922901 Incisor I Pulsed ND:Yag Laser SystemBuckman Co., Inc. · 1992
  2. 5 generations backK972325 Pulsemaster 1000 ST Dental Laser SystemAmerican Dental Technologies, Inc. · 1997
  3. 4 generations backK983058 Ceralas D Laser System, Model # Ceralas D15Ceram Optec, Inc. · 1998
  4. 3 generations backK991891 Ceralas Diode Laser System, Model Ceralas D15Ceram Optec, Inc. · 1999
  5. 2 generations backK053161 SirolaserSirona Dental Systems GmbH · 2006
  6. 1 generation backK063384 Diodent Micro Dental Laser System, Models 810 and 980Hoya Conbio, Inc. · 2007
  7. This deviceK073332 V-Raser Diode Laser SystemHoya Conbio, Inc. · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K922901Incisor I Pulsed ND:Yag Laser SystemBuckman Co., Inc.1992—
−5K972325Pulsemaster 1000 ST Dental Laser SystemAmerican Dental Technologies, Inc.1997—
−4K983058Ceralas D Laser System, Model # Ceralas D15Ceram Optec, Inc.1998—
−3K991891Ceralas Diode Laser System, Model Ceralas D15Ceram Optec, Inc.1999—
−2K053161SirolaserSirona Dental Systems GmbH2006—
−1K063384Diodent Micro Dental Laser System, Models 810 and 980Hoya Conbio, Inc.2007—
0 (this device)K073332V-Raser Diode Laser SystemHoya Conbio, Inc.2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198810
199010
199410
199530
199620
199730
199840
199910
200110
200310
200410
200510
FIG. 1 — Lineage of K073332, 1992–2008Source: 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 GEX? 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 GEX device

  1. #1 K222064 The Alma Soprano Titaniumscore 38.1 · 24 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K063384Diodent Micro Dental Laser System, Models 810 and 980
Summary page 1
…ended to destroy or coagulate tissue by light energy emitted by argon. Equivalent Device: Diodent Micro 980 (K063384), Iridex Varilite (K041930), Device Description: The V-RASER Diode System is a modified Diodent Micro…
Hoya Conbio, Inc.2007—
*K041930Varilite Laser System
Summary page 1
…te tissue by light energy emitted by argon. Equivalent Device: Diodent Micro 980 (K063384), Iridex Varilite (K041930), Device Description: The V-RASER Diode System is a modified Diodent Micro…
Iridex Corporation2004—

Also cleared against K063384: 4 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 16 years and passes through 5 companies; a new generation was cleared every 1.2 years on median.
  • None of the 26 ancestors has a recall.
  • 4 other devices also cite its predicate K063384.

How does its category compare?

All GEX devices

GEX Powered Laser Surgical Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · GEX

83in 2025

2007: 732008: 1072009: 692010: 502011: 412012: 452013: 462014: 612015: 472016: 512017: 672018: 512019: 412020: 522021: 532022: 602023: 522024: 822025: 832026 (partial year): 57
2007high 107 (2008) · low 41 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEX

90in 2025

2007: 79 days median2008: 86 days median2009: 100 days median2010: 96 days median2011: 83 days median2012: 118 days median2013: 144 days median2014: 147 days median2015: 112 days median2016: 114 days median2017: 90 days median2018: 78 days median2019: 88 days median2020: 90 days median2021: 123 days median2022: 152 days median2023: 87 days median2024: 90 days median2025: 90 days median2026 (partial year): 90 days median
2007high 152 (2022) · low 78 (2018)2026

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

Recalls per year · GEX

3in 2024

2007: 92008: 22010: 42011: 182012: 52013: 32014: 62016: 12017: 5, 1 Class I2018: 52019: 62020: 12023: 62024: 32026 (partial year): 2
2007high 18 (2011) · low 0 (2009)2026

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

Adverse event reports per year · GEX

2,720in 2025

2007: 3422008: 2322009: 2092010: 1,7112011: 3,0242012: 2,0002013: 2,2362014: 2,0362015: 2,0992016: 2,5852017: 2,9772018: 3,5252019: 2,7092020: 2,1832021: 3,4652022: 2,2882023: 2,3372024: 2,1872025: 2,720
2007high 3,525 (2018) · low 209 (2009)2025

MAUDE reports naming product code GEX, 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
200773799342
2008107862232
2009691000209
2010509641,711
20114183183,024
20124511852,000
20134614432,236
20146114762,036
20154711202,099
20165111412,585
201767905 (1)2,977
2018517853,525
2019418862,709
2020529012,183
20215312303,465
20226015202,288
2023528762,337
2024829032,187
2025839002,720
202657902—

What is it indicated for?

The V-Raser is intended for Incision, excision, ablation, vaporization and coagulation of soft tissue.

Treatment of vascular lesions.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K073332: V-Raser Diode Laser System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K073332

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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