510(k) Report

510(k) · Cleared

Cleared

Litho Laser System

K091909510(k) TraditionalCleared Jul 9, 200914-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

Quanta System Spa · GEX Powered Laser Surgical Instrument

Cleared on Jul 9, 2009 as substantially equivalent to K033437 (Allmed Systems, Inc., 2004) after a 14-day review. Its family tree reaches back 1 generation to 2004. 18 later devices descend from it.

Decided
Jul 9, 2009
Review
14 days
Class
Class II
Product code
GEX
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K033437 (2004). 18 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2014: 2 descendants cleared2017: 3 descendants cleared2016: 1 descendant cleared2015: 1 descendant cleared2026: 2 descendants cleared2018: 3 descendants cleared2023: 1 descendant cleared2019: 1 descendant cleared2020: 2 descendants cleared2024: 1 descendant cleared2025: 1 descendant clearedK033437 · Sphinx Laser Systems · Allmed Systems, Inc. · 2004200020052010201520202025
Descendants, by generation 1 generation forward: 2 descendants2 generations forward: 4 descendants3 generations forward: 3 descendants4 generations forward: 2 descendants5 generations forward: 3 descendants6 generations forward: 2 descendants7 generations forward: 2 descendants K033437 · Sphinx Laser Systems · Allmed Systems, Inc. · 20040+5
  1. Root · 1 generation backK033437 Sphinx Laser SystemsAllmed Systems, Inc. · 2004
  2. This deviceK091909 Litho Laser SystemQuanta System Spa · 2009
  3. Descendant · cites it directly · 14 of its ownK141101 LITHOQuanta System Spa · 2014
  4. Descendant · 2 generations on · 12 of its ownK163009 LithoQuanta System Spa · 2016
  5. Descendant · 3 generations on · 9 of its ownK170331 Cyber HoQuanta System Spa · 2017
  6. Descendant · 4 generations on · 8 of its ownK172025 Litho 60Quanta System Spa · 2017
  7. Descendant · 5 generations on · 6 of its ownK180922 Empower H100, Cyber Ho 100, Litho 100Quanta System Spa · 2018

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

2014: 22015: 12016: 12017: 32018: 32019: 12020: 22023: 12024: 12025: 12026: 2
2014high 3 (2017) · low 0 (2021)2026

Most influential descendants

Showing 5 of 18 · See all
  • K141101LITHOQuanta System Spa · 2014 · cites it directly14descendants
  • K163009LithoQuanta System Spa · 2016 · 2 generations on12descendants
  • K170331Cyber HoQuanta System Spa · 2017 · 3 generations on9descendants
  • K172025Litho 60Quanta System Spa · 2017 · 4 generations on8descendants
  • K180922Empower H100, Cyber Ho 100, Litho 100Quanta System Spa · 2018 · 5 generations on6descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K033437Sphinx Laser SystemsAllmed Systems, Inc.2004—
0 (this device)K091909Litho Laser SystemQuanta System Spa2009—
+1K141101LITHOQuanta System Spa2014—
+2K163009LithoQuanta System Spa2016—
+3K170331Cyber HoQuanta System Spa2017—
+4K172025Litho 60Quanta System Spa2017—
+5K180922Empower H100, Cyber Ho 100, Litho 100Quanta System Spa2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201510
201610
201730
201830
201910
202020
202310
202410
202510
202620
FIG. 1 — Lineage of K091909, 2004–2026Source: 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.

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? (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
*K033437Sphinx Laser Systems
Summary page 1
…ermatology Classification Name: Instrument, surgical, powered, laser Predicate Devices: - AllMed System Sphinx Laser System (K033437); Intended Use / 2.1 gm Applications: Indications for Use: The LITHO laser system and its fiber…
Allmed Systems, Inc.2004—

Also cleared against K033437: 4 other devices →

What descends from it? (18)

See all 18

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

NumberDeviceApplicantDecidedDescendants
K141101LITHOQuanta System Spa201414
K141403Litho DK30Quanta System Spa20142

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?

  • Its one ancestor has no recall.
  • Of its descendants, K141101 (Quanta System Spa, 2014) has gone furthest, with 14 descendants of its own.
  • 4 other devices also cite its predicate K033437.

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. 2009, 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?

2.1 gm Applications: The LITHO laser system 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 hemostasis of soft tissue in use in medical specialties including: Urology, Urinary Lithotnpsy, Gasteroenterology, Arthroscopy, Discetomy Pulmonary, Gynecology, ENT, Dermatology, Plastic Surgery and General Surgery. Urology…

Read the full statement (478 words)

2.1 gm Applications:

The LITHO laser system 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 hemostasis of soft tissue in use in medical specialties including: Urology, Urinary Lithotnpsy, Gasteroenterology, Arthroscopy, Discetomy Pulmonary, Gynecology, ENT, Dermatology, Plastic Surgery and General Surgery.

Urology

Open and endoscopic surgery (incision, excision, resection, ablation, vaporization, coagulation and hemostasis) including:

Urethral Strictures

Bladder Neck Incisions (BNI)

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

Ablation of Benign Prostatic Hypertrophy (B9fP), (r~off)

Transurethral incision of the prostate (TUIP)

Holmiurn Laser Resection of the Prostrate (HoLRP)

Holmium Laser Enuculeation of the Prostate (HoLEP)

Holmiurm 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( her gj4i~e wire cannot be passed.

Gasteroenterlogv

Open and endoscopic gasteroenterlogy surgery (incision,. excision, resection,- ablation, vaporization, coagulation and hemostasis ) including:

Appendectomy

Polyps

Biopsy

Gall Bladder calculi

Biliary/Bile duct calculi

Ulcers

Gastric ulcers

Duodenal ulcers

Non Bleeding Ulcers

Pancreatitas

Hemorrhoids

Cholecystectomy

Benign and Malignant Neoplasm

Angiodysplasia

Colorectal cancer

Telangiectasias

Telangiectasias of the Osler-Weber-Renu disease

Vascular Malformation

Gastritis

Esoph'agitis

Esophageal ulcers

Varices

Colitis

Mallory-Weiss tear

Gastric Erosions

Arthroscon3

Arthroscopy/Orthopedic 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

Countouring 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 Debuidement

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

Pulmonary

Open and endoscopic pulmonary surgery (incision, excision, resection, ablation, vaporization, coagulation and hemostasis of soft tissue)

Gynecologv

Open and laparoscopic gynecological surgery (incision, excision, resection, ablation, vaporization, coagulation and hemostasis) of soft tissue

ENT

Endoscopic endonasal surgery (incision, excision, resection, ablation, vaporization, coagulation and hemostasis of soft tissue and cartilage) including:

Endonasal/sinus Surgery

Partial turbinectomy

Polypectomy

Dacryocystorhinostomy

Frontal Sinusotomy

Ethmoidectomy

Maxillary antrostomy

Functional endoscopic sinus surgery

Dermatology and Plastic Surgery

Incision, excision, resection, ablation, vaporization, coagulation and hemostasis of soft,mucosal, fatty and cartilaginous tissue, in therapeutic plastic, dermatologic and aesthetic surgical procedures including:

Basal Cell Carcinomas

Lesions of skin and subcutaneous tissue

Skin tags

Plantar warts

Lesions of skin and subcutaneous tissue

Port Wine Stains

Papillomas

General Surgery

Open, laparoscopic and endoscopic surgery (incision, excision, resection, ablation, vaporization, coagulation and hemostasis) including:

Appendectomy

Skin incision

Excision of external and internal lesions

Complete of partial resection of internal organs, tumors-and lesions

Biopsy

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K091909: Litho 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/K091909

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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