510(k) · Cleared
Recalled · Class II · 2014Waterlase MD Turbo Plus Model 7200XXX
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Biolase Technology, Inc. · GEX Powered Laser Surgical Instrument
Cleared on Aug 11, 2010 as substantially equivalent to K031140 (Biolase Technology, Inc., 2004) and 10 other predicates after a 61-day review. Its family tree reaches back 10 generations to 1992. 25 later devices descend from it. It has been recalled once.
- Decided
- Aug 11, 2010
- Review
- 61 days
- Class
- Class II
- Product code
- GEX
- Recalls
- 1
- Predicates
- 11
Its longest line of descent runs back 10 generations to K910422 (1992). 126 ancestors in all, the oldest K820106 (1982). 25 later devices descend from it, 3 citing it directly.
- Root · 10 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
- 6 generations between
- 3 generations backK033172 Candela Gentleyag Family of Laser SystemsCandela Corp. · 2003
- 2 generations backK050293 Fotona XP Plus ND: Yag Family of Laser Systems, Fontona Dualis XP…Fotona D.D. · 2005
- 1 generation backK070355 Fotona Fidelis Iii ER:Yag/ND:Yag Laser System FamilyFotona D.D. · 2008
- This deviceK101658 Waterlase MD Turbo Plus Model 7200XXXBiolase Technology, Inc. · 2010
- Descendant · cites it directly · 21 of its ownK161669 Waterlase ExpressBiolase, Inc. · 2016
- Descendant · cites it directly · 19 of its ownK190319 Waterlase Laser System FamilyBiolase, Inc. · 2019
- Descendant · 2 generations on · 11 of its ownK193656 SkyPulseFotona D.O.O. · 2020
- Descendant · 2 generations on · 8 of its ownK193661 LightWalker Laser System FamilyFotona D.O.O. · 2020
- Descendant · 3 generations on · 7 of its ownK202985 LightWalker Laser System FamilyFotona D.O.O. · 2021
Show all 10 generations
- Root · 10 generations backK910422 Model RD-1200 Ruby Laser SystemSpectrum Medical Technologies, Inc. · 1992
- 9 generations backK961279 Sharplan Lasers, Inc. Ruby Laser SystemSharplan Lasers, Inc. · 1996
- 8 generations backK962446 Sharplan Ruby Laser SystemSharplan Lasers, Inc. · 1997
- 7 generations backK974536 Photoderm HR SystemEsc Medical Systems, Ltd. · 1998
- 6 generations backK991935 Epilight Hair Removal System, Photoderm HR SystemEsc Medical Systems, Ltd. · 2000
- 5 generations backK014040 Family of Altus Medical Modified Coolglide Aesthetic Lasers, Models…Altus Medical, Inc. · 2002
- 4 generations backK023193 Candela Gentle Yag Laser SystemCandela Corp. · 2002
- 3 generations backK033172 Candela Gentleyag Family of Laser SystemsCandela Corp. · 2003
- 2 generations backK050293 Fotona XP Plus ND: Yag Family of Laser Systems, Fontona Dualis XP…Fotona D.D. · 2005
- 1 generation backK070355 Fotona Fidelis Iii ER:Yag/ND:Yag Laser System FamilyFotona D.D. · 2008
- This deviceK101658 Waterlase MD Turbo Plus Model 7200XXXBiolase Technology, Inc. · 2010
Showing 5 of 25 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 25 · See all- K161669Waterlase ExpressBiolase, Inc. · 2016 · cites it directly21descendants
- K190319Waterlase Laser System FamilyBiolase, Inc. · 2019 · cites it directly19descendants
- K193656SkyPulseFotona D.O.O. · 2020 · 2 generations on11descendants
- K193661LightWalker Laser System FamilyFotona D.O.O. · 2020 · 2 generations on8descendants
- K202985LightWalker Laser System FamilyFotona D.O.O. · 2021 · 3 generations on7descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K910422 | Model RD-1200 Ruby Laser System | Spectrum Medical Technologies, Inc. | 1992 | — |
| −9 | K961279 | Sharplan Lasers, Inc. Ruby Laser System | Sharplan Lasers, Inc. | 1996 | — |
| −8 | K962446 | Sharplan Ruby Laser System | Sharplan Lasers, Inc. | 1997 | — |
| −7 | K974536 | Photoderm HR System | Esc Medical Systems, Ltd. | 1998 | — |
| −6 | K991935 | Epilight Hair Removal System, Photoderm HR System | Esc Medical Systems, Ltd. | 2000 | — |
| −5 | K014040 | Family of Altus Medical Modified Coolglide Aesthetic Lasers, Models Coolglide… | Altus Medical, Inc. | 2002 | — |
| −4 | K023193 | Candela Gentle Yag Laser System | Candela Corp. | 2002 | — |
| −3 | K033172 | Candela Gentleyag Family of Laser Systems | Candela Corp. | 2003 | — |
| −2 | K050293 | Fotona XP Plus ND: Yag Family of Laser Systems, Fontona Dualis XP Plus ND: Yag… | Fotona D.D. | 2005 | — |
| −1 | K070355 | Fotona Fidelis Iii ER:Yag/ND:Yag Laser System Family | Fotona D.D. | 2008 | — |
| 0 (this device) | K101658 | Waterlase MD Turbo Plus Model 7200XXX | Biolase Technology, Inc. | 2010 | — |
| +1 | K161669 | Waterlase Express | Biolase, Inc. | 2016 | — |
| +1 | K190319 | Waterlase Laser System Family | Biolase, Inc. | 2019 | — |
| +2 | K193656 | SkyPulse | Fotona D.O.O. | 2020 | — |
| +2 | K193661 | LightWalker Laser System Family | Fotona D.O.O. | 2020 | — |
| +3 | K202985 | LightWalker Laser System Family | Fotona D.O.O. | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1982 | 1 | 0 |
| 1988 | 1 | 0 |
| 1990 | 1 | 0 |
| 1991 | 4 | 0 |
| 1993 | 5 | 0 |
| 1994 | 8 | 0 |
| 1995 | 6 | 0 |
| 1996 | 8 | 0 |
| 1997 | 9 | 0 |
| 1998 | 8 | 0 |
| 1999 | 5 | 0 |
| 2000 | 12 | 0 |
| 2001 | 11 | 0 |
| 2002 | 14 | 0 |
| 2003 | 7 | 0 |
| 2004 | 6 | 0 |
| 2005 | 4 | 0 |
| 2006 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 3 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 1 | 0 |
| 2015 | 1 | 0 |
| 2016 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 3 | 0 |
| 2022 | 3 | 0 |
| 2023 | 2 | 0 |
| 2024 | 3 | 0 |
| 2025 | 4 | 0 |
| 2026 | 4 | 0 |
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 K222064 The Alma Soprano Titaniumscore 38.1 · 24 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (11)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K031140 | WaterlaseSummary page 1…EX, MXF, DZI, a Class II device Equivalent Devices: Waterlase®MD Biolase Technology, Inc. K031140, July 7, 2004; KO071363, February 12, 2008 Waterlase®MD Turbo… | 2004 |
| * | K071363 | Waterlase and Waterlase MDSummary page 4…Conclusion: The indications included herein are the same as the indications that have been previously cleared by the FDA for the Waterlase®MD predicates under K03 1140, K071363, K090181, K(083927, and 1(091746, as well as other dental laser predicates, such as 1(001527,1(070355, K983 100, 1(000805, K(0301… | 2008 |
| * | K090181 | Waterlase MDSummary page 1…071363, February 12, 2008 Waterlase®MD Turbo Biolase Technology, Inc. K090181, February 11, 2009; K(083927, October 1,2009; K091 746, December 7, 2009 Device Description: T… | 2009 |
| * | K083927 | Waterlase MDSummary page 1…Waterlase®MD Turbo Biolase Technology, Inc. K090181, February 11, 2009; K(083927, October 1,2009; K091 746, December 7, 2009 Device Description: The Waterlase®MIJTurbo Plus is… | 2009 |
| * | K091746 | Waterlase MD, Model 7100102Summary page 1…Biolase Technology, Inc. K090181, February 11, 2009; K(083927, October 1,2009; K091 746, December 7, 2009 Device Description: The Waterlase®MIJTurbo Plus is a dental laser device indicated for incision, excision, re… | 2009 |
| * | K030146 | Kavo Key Laser 1242 and Kavo Key Laser 1243+Summary page 4…(predicate, K09018 1). In addition, the Waterlase®MIJ Turbo Plus operated at 600 mJ per pulse is also equivalent to the other predicated devices cleared by the FDA under K030 146 and K070355. For the additional pulse frequencies of 75 and 100Hz, the Waterlase®MD Turbo Plus device was determined safe and eff… | 2005 |
| * | K070355 | Fotona Fidelis Iii ER:Yag/ND:Yag Laser System FamilySummary page 4…09018 1). In addition, the Waterlase®MIJ Turbo Plus operated at 600 mJ per pulse is also equivalent to the other predicated devices cleared by the FDA under K030 146 and K070355. For the additional pulse frequencies of 75 and 100Hz, the Waterlase®MD Turbo Plus device was determined safe and effective throu… | 2008 |
| * | K001527 | Fotona Fidelis ER: Yag Laser System and AccesoriesSummary page 4…eviously cleared by the FDA for the Waterlase®MD predicates under K03 1140, K071363, K090181, K(083927, and 1(091746, as well as other dental laser predicates, such as 1(001527,1(070355, K983 100, 1(000805, K(030146, and 1(073074. No clinical performance data is required for this submission. Therefore, su… | 2000 |
| * | K983100 | Kavo Key Laser 1242Summary page 4…by the FDA for the Waterlase®MD predicates under K03 1140, K071363, K090181, K(083927, and 1(091746, as well as other dental laser predicates, such as 1(001527,1(070355, K983 100, 1(000805, K(030146, and 1(073074. No clinical performance data is required for this submission. Therefore, substantial equivalen… | 1999 |
| * | K000805 | Kavo K.E.Y. Laser 1242Summary page 4…or the Waterlase®MD predicates under K03 1140, K071363, K090181, K(083927, and 1(091746, as well as other dental laser predicates, such as 1(001527,1(070355, K983 100, 1(000805, K(030146, and 1(073074. No clinical performance data is required for this submission. Therefore, substantial equivalency for the… | 2000 |
| * | K073074 | Key Laser Iii 1243 US with DetectSummary page 4…icates under K03 1140, K071363, K090181, K(083927, and 1(091746, as well as other dental laser predicates, such as 1(001527,1(070355, K983 100, 1(000805, K(030146, and 1(073074. No clinical performance data is required for this submission. Therefore, substantial equivalency for the Waterlase®MD Turbo Plus… | 2008 |
What descends from it? (25)
See all 253 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jun 12, 2014 | Class II | Z-2263-2014 | Under Investigation by firm | Biolase is recalling the WaterLase iPlus Dental Laser System because of a discrepancy present in the user interface software (version 1.7). If an error occurs in the procedure screen, the air setting will change to 1% and OFF. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 18 years and passes through 7 companies; a new generation was cleared every 1.7 years on median.
- 6 of the 126 ancestors have a recall of any class.
- Of its descendants, K161669 (Biolase, Inc., 2016) has gone furthest, with 21 descendants of its own.
- 3 other devices also cite its predicate K031140.
How does its category compare?
All GEX devicesGEX Powered Laser Surgical Instrument: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · GEX
83in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GEX
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GEX
3in 2024
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · GEX
2,720in 2025
MAUDE reports naming product code GEX, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 73 | 79 | 9 | 342 |
| 2008 | 107 | 86 | 2 | 232 |
| 2009 | 69 | 100 | 0 | 209 |
| 2010 | 50 | 96 | 4 | 1,711 |
| 2011 | 41 | 83 | 18 | 3,024 |
| 2012 | 45 | 118 | 5 | 2,000 |
| 2013 | 46 | 144 | 3 | 2,236 |
| 2014 | 61 | 147 | 6 | 2,036 |
| 2015 | 47 | 112 | 0 | 2,099 |
| 2016 | 51 | 114 | 1 | 2,585 |
| 2017 | 67 | 90 | 5 (1) | 2,977 |
| 2018 | 51 | 78 | 5 | 3,525 |
| 2019 | 41 | 88 | 6 | 2,709 |
| 2020 | 52 | 90 | 1 | 2,183 |
| 2021 | 53 | 123 | 0 | 3,465 |
| 2022 | 60 | 152 | 0 | 2,288 |
| 2023 | 52 | 87 | 6 | 2,337 |
| 2024 | 82 | 90 | 3 | 2,187 |
| 2025 | 83 | 90 | 0 | 2,720 |
| 2026 | 57 | 90 | 2 | — |
What is it indicated for?
General Indications* * Class I, II, III, IV and V cavity preparation * Caries removal * Hard tissue surface roughening or etching * Enameloplasty, excavation of pits and fissures for placement of sealants *For use on adult and pediatric patients Root Canal Hard Tissue Indications * Tooth preparation to obtain access to root canal * Root canal preparation including enlargement * Root canal debridement and cleaning Root Canal Disinfection * Laser root…
Read the full statement (570 words)
General Indications*
* Class I, II, III, IV and V cavity preparation
* Caries removal
* Hard tissue surface roughening or etching
* Enameloplasty, excavation of pits and fissures for placement of sealants
*For use on adult and pediatric patients
Root Canal Hard Tissue Indications
* Tooth preparation to obtain access to root canal
* Root canal preparation including enlargement
* Root canal debridement and cleaning
Root Canal Disinfection
* Laser root canal disinfection after endodontic treatment
Endodontic Surgery (Root Amputation) Indications
* Flap preparation - incision of soft tissue to prepare a flap and expose the bone.
* Cutting bone to prepare a window access to the apex (apices) of the root(s).
* Apicoectomy - amputation of the root end,
* Root end preparation for retrofill amalgam or composite..
* Removal of pathological tissues (i.e., cysts, neoplasm or abscess) and hyperplastic tissues (i.e., granulation tissue) from around the apex
NOTE: Any tissue growth (i.e., cyst, neoplasm or other lesions) must be submitted to a qualified laboratory for histopathological evaluation.
Bone Surgical Indications
* Cutting, shaving, contouring and resection of oral osseous tissues (bone)
* Osteotomy
Soft Tissue Indications including Pulpal Tissues*
Incision, excision, vaporization, ablation and coagulation of oral soft tissues, including:
* Excisional and incisional biopsies
* Exposure of unerupted teeth
* Fibroma removal
* Flap preparation - incision of soft tissue to prepare a flap and expose the bone.
* Flap preparation - incision of soft tissue to prepare a flap and expose unerupted teeth (hard and soft tissue impactions)
* Frenectomy and frenotomy
* Gingival troughing for crown impressions
* Gingivectomy
* Gingivoplasty
* Gingival incision and excision
* Hemostasis
* Implant recovery
* Incision and drainage of abscesses
* Laser soft tissue curettage of the post-extraction tooth sockets and the periapical area during apical surgery
* Leukoplakia
* Operculectomy
* Oral papillectomies
* Operculectomy
* Oral papillectomies
* Pulpotomy
* Pulp extirpation
* Pulpotomy as an adjunct to root canal therapy
* Root canal debridement and cleaning
* Reduction of gingival hypertrophy
* Removal of pathological tissues (i.e., cysts, neoplasm or abscess) and hyperplastic tissues (i.e., granulation tissue) from around the apex
NOTE: Any tissue growth (i.e., cyst, neoplasm or other lesions) must be submitted to a qualified laboratory for histopathological evaluation.
* Soft tissue crown lengthening
* Treatment of canker sores, herpetic and aphthous ulcers of the oral mucosa
* Vestibuloplasty
*For use on adult and pediatric patient
Laser Periodontal Procedures
* Full thickness flap
* Partial thickness flap
* Split thickness flap
* Laser soft tissue curettage
* Laser removal of diseased, infected, inflamed and necrosed soft tissue within the periodontal pocket
* Removal of highly inflamed edematous tissue affected by bacterial penetration of the pocket lining junctional epithelium
* Removal of granulation tissue from bony defects
* Sulcular debridement (removal of diseased, infected, inflamed or necrosed soft tissue in the periodontal pocket to improve clinical indices including gingival index, gingival bleeding index, probe depth, attachment loss and tooth mobility)
* Osteoplasty and osseous recontouring (removal of bone to correct osseous defects and create physiologic osseous contours)
* Ostectomy (resection of bone to restore bony architecture, resection of bone for grafting, etc.)
* Osseous crown lengthening
* Removal of subgingival calculi in periodontal pockets with periodontitis by closed or open curettage
Waterlase MD Er,Cr:YSGG assisted new attachment procedure (cementum-mediated periodontal ligament new-attachment to the root surface in the absence of long junctional epithelium)
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K101658 · printed Nov 6, 2026
Cite this page
510(k) Report. “K101658: Waterlase MD Turbo Plus Model 7200XXX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101658
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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