510(k) Report

510(k) · Cleared

Cleared

Holmium Medical Laser

K231718510(k) TraditionalCleared Aug 18, 202366-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

Allengers Global Healthcare Private Limited · GEX Powered Laser Surgical Instrument

Cleared on Aug 18, 2023 as substantially equivalent to K192600 (Quanta System Spa, 2020) and 2 other predicates after a 66-day review. Its family tree reaches back 12 generations to 1994.

Decided
Aug 18, 2023
Review
66 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
3

Its longest line of descent runs back 12 generations to K936109 (1994). 40 ancestors in all, the oldest K853620 (1986). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2018: 1 other ancestor2014: 1 other ancestor2009: 1 other ancestor2004: 1 other ancestor2000: 1 other ancestor1999: 1 other ancestor1995: 4 other ancestors1998: 3 other ancestors1996: 2 other ancestors1994: 3 other ancestors1993: 1 other ancestor1992: 2 other ancestors1991: 3 other ancestors1990: 1 other ancestor1989: 1 other ancestor1997: 1 other ancestor1986: 1 other ancestorReference device: K170121 · Lumenis Family of Holmium Surgical Lasers and Delivery Devices and Accessories · Lumenis, Ltd. · 2017 · recalledK936109 · Sharplan Model 1120 CO2 Surgical Laser · Sharplan Lasers, Inc. · 1994K960521 · Sharplan Lasers, Inc. Silktouch Flash Scanner · Sharplan Lasers, Inc. · 1996K963339 · Coherent Ultrapulse CO2 Surgical Lasers · Coherent Medical Group · 1997K974789 · Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and L · Lumenis, Inc. · 1998K990947 · Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO: Yag/ND: Yag Surgical Lasers and Delivery · Lumenis, Inc. · 1999K011703 · Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength (HO:Yag/ND:Yag) Surgical Lasers and Delivery Devices · Lumenis · 2001 · recalledK140388 · Lumenis Pulse 120H · Lumenis, Ltd. · 2014×2: 2 generations cleared close together, K163009 (2016), K170331 (2017) K172025 · Litho 60 · Quanta System Spa · 2017K180922 · Empower H100, Cyber Ho 100, Litho 100 · Quanta System Spa · 2018K192600 · Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60 · Quanta System Spa · 20201990200020102020
  1. Root · 12 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
  2. 8 generations between
  3. 3 generations backK172025 Litho 60Quanta System Spa · 2017
  4. 2 generations backK180922 Empower H100, Cyber Ho 100, Litho 100Quanta System Spa · 2018
  5. 1 generation backK192600 Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60Quanta System Spa · 2020
  6. This deviceK231718 Holmium Medical LaserAllengers Global Healthcare Private Limited · 2023
Show all 12 generations
  1. Root · 12 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
  2. 11 generations backK960521 Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc. · 1996
  3. 10 generations backK963339 Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group · 1997
  4. 9 generations backK974789 Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc. · 1998
  5. 8 generations backK990947 Modified Versapulse Select Single Wavelength, HO: Yag and Dual…Lumenis, Inc. · 1999
  6. 7 generations backK011703 Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength…Lumenis · 2001 · Recalled
  7. 6 generations backK140388 Lumenis Pulse 120HLumenis, Ltd. · 2014
  8. 5 generations backK163009 LithoQuanta System Spa · 2016
  9. 4 generations backK170331 Cyber HoQuanta System Spa · 2017
  10. 3 generations backK172025 Litho 60Quanta System Spa · 2017
  11. 2 generations backK180922 Empower H100, Cyber Ho 100, Litho 100Quanta System Spa · 2018
  12. 1 generation backK192600 Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60Quanta System Spa · 2020
  13. This deviceK231718 Holmium Medical LaserAllengers Global Healthcare Private Limited · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K936109Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc.1994—
−11K960521Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc.1996—
−10K963339Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group1997—
−9K974789Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc.1998—
−8K990947Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO…Lumenis, Inc.1999—
−7K011703Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength…Lumenis20012
−6K140388Lumenis Pulse 120HLumenis, Ltd.2014—
−5K163009LithoQuanta System Spa2016—
−4K170331Cyber HoQuanta System Spa2017—
−3K172025Litho 60Quanta System Spa2017—
−2K180922Empower H100, Cyber Ho 100, Litho 100Quanta System Spa2018—
−1K192600Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60Quanta System Spa2020—
0 (this device)K231718Holmium Medical LaserAllengers Global Healthcare Private Limited2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198610
198910
199010
199130
199220
199310
199430
199540
199620
199710
199830
199910
200010
200410
200910
201410
201810
FIG. 1 — Lineage of K231718, 1994–2023Source: 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
Get a 510(k) Report

What was it cleared against? (3)

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
*K192600Cyber Ho 60, Cyber Ho 100, Litho 100, Litho 60
Summary page 7
…21 CFR 878.4810 Product Code GEX Panel General and Plastic Surgery Predicate Devices Cyber Ho 100 (K192600)-Quanta system spa Empower H65(K180423), Litho(K163009)- Quanta system spa Reference Devices…
Quanta System Spa2020—
*K180423Empower H65
Summary page 7
…General and Plastic Surgery Predicate Devices Cyber Ho 100 (K192600)-Quanta system spa Empower H65(K180423), Litho(K163009)- Quanta system spa Reference Devices Lumenis Pulse 120H (K170121)-Lumenis Ltd…
Quanta System Spa2018—
*K163009Litho
Summary page 7
…General and Plastic Surgery Predicate Devices Cyber Ho 100 (K192600)-Quanta system spa Empower H65(K180423), Litho(K163009)- Quanta system spa Reference Devices Lumenis Pulse 120H (K170121)-Lumenis Ltd. Allengers…
Quanta System Spa2016—
†K170121Lumenis Family of Holmium Surgical Lasers and Delivery Devices and AccessoriesLumenis, Ltd.20171

Also cleared against K192600: 2 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 29 years and passes through 7 companies; a new generation was cleared every 1.8 years on median.
  • 1 of the 40 ancestors has a recall of any class.
  • 2 other devices also cite its predicate K192600.

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. 2023, 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 Holmium Medical Laser and its fiber optic delivery system are intended for use in surgical procedures using open, laparoscopic and endoscopic incision, excision, resection, ablation, vaporization, coagulation and haemostasis of soft tissue in use in medical specialties including: Urology, Urinary Lithotripsy, Gastroenterology, Arthroscopy, Discectomy, Gynecology, ENT, Pulmonary Surgery and General Surgery. Urology Open and endoscopic surgery…

Read the full statement (485 words)

The Holmium Medical Laser and its fiber optic delivery system are intended for use in surgical procedures using open,

laparoscopic and endoscopic incision, excision, resection, ablation, vaporization, coagulation and haemostasis of soft

tissue in use in medical specialties including: Urology, Urinary Lithotripsy, Gastroenterology, Arthroscopy, Discectomy,

Gynecology, ENT, Pulmonary Surgery and General Surgery.

Urology

Open and endoscopic surgery (incision, excision, resection, ablation, vaporization, coagulation and haemostasis)

including:

* Urethral Strictures

* Bladder Neck Incisions (BNI)

* Ablation and resection of Bladder Tumors, Uretheral Tumors and Ureteral Tumors,

* Ablation of Benign Prostatic Hypertrophy (BPH),

* Transurethral incision of the prostate (TUIP)

* Holmium Laser Resection of the Prostrate (HoLRP)

* Holmium Laser Enucleation of the Prostate (HoLEP)

* Holmium laser Ablation of the Prostate (HoLAP)

* Condylomas

* Lesions of external genitalia

Lithotripsy and Percutaneous Urinary Lithotripsy

* Endoscopic fragmentation of urethral, ureteral, bladder and renal calculi including cystine, calcium oxalate,

monohydrate and calcium oxalate

* dehydrate stones.

* Endoscopic fragmentation of kidney calculi.

* Treatment of distal impacted fragments of steinstrasse when guide wire cannot be passed.

Gastroenterology

Open and endoscopic Gastroenterology surgery (incision, excision, resection, ablation, vaporization, coagulation and

haemostasis) including:

* Appendectomy

* Polyps

* Biopsy

* Gall Bladder calculi

* Biliary/Bile duct calculi

* Ulcers

* Gastric ulcers

* Duodenal ulcers

* Non Bleeding Ulcers

* Pancreatitas

* Haemorrhoids

* Cholecystectomy

* Benign and Malignant Neoplasm

* Angiodysplasia

* Colorectal cancer

* Telangiectasias

* Telangiectasias of the Osler-Weber-Renu disease

* Vascular Malformation

* Gastritis

* Esophagitis

* Esophageal ulcers

* Varices

* Colitis

* Mallory-Weiss tear

* Gastric Erosions

Arthroscopy

Arthroscopy/Orthopaedic surgery (excision, ablation and coagulation of soft and cartilaginous tissue) in small and large

joints of the body, excluding the spine but including:

* Ligament and tendon Release

* Contouring and sculpting of articular surfaces

* Capsulectomy in the Knee

* Chondreplasty in the Knee

* Debridement of inflamed synovial tissue

* Chondromalacia Ablation

* Chondromalacia and tears

* Plica Removal

* Meniscectomy

* Loose Body Debridement

* Lateral retinecular release

Ablation of soft, cartilaginous and bony tissue in Minimal Invasive Spinal Surgery including

* Percutaneous Laser Disc Decompression/Discectomy of the L4-5 and L5-SI lumbar discs, including Foraminoplasty

Percutaneous Cervical Disc Decompression/Discectomy

Percutaneous Thoracic Disc Decompression/Discectomy

Gynaecology

Open and laparoscopic gynaecological surgery (incision, excisio n, resection, ablation, vaporization, coagulation and

haemostasis) of soft tissue

ENT

Endoscopic endonasal surgery (incision, excision, resection, ablation, vaporization, coagulation and haemostasis of soft

tissue and cartilage) including:

* Endonasal/sinus Surgery

* Partial turbinectomy

* Polypectomy

* Dacryocystorhinostomy

* Frontal Sinusotomy

* Ethmoidectomy

* Maxillary antrostomy

* Functional endoscopic sinus surgery

Pulmonary Surgery

Open and endoscopic pulmonary surgery (cutting, vaporization, incision, excision and coagulation of soft tissue)

General Surgery

Open, laparoscopic and endoscopic surgery (incision, excision, resection, ablation, vaporization,coagulation and

haemostasis) including:

* Appendectomy

* Skin incision

* Excision of external and internal lesions

* Complete or partial resection of internal organs, tumors and lesions

* Biopsy

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231718: Holmium Medical Laser.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231718

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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