510(k) Report

510(k) · Cleared

Cleared

neXus Ultrasonic Surgical Aspirator System

K231117510(k) SpecialCleared Jun 23, 202364-day reviewClass U

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

Misonix, LLC, A Bioventus Company · LFL Instrument, Ultrasonic Surgical

Cleared on Jun 23, 2023 as substantially equivalent to K221235 (Misonix, Inc., 2022) after a 64-day review. Its family tree reaches back 9 generations to 1988. 1 later device descends from it.

Decided
Jun 23, 2023
Review
64 days
Class
Class U
Product code
LFL
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K884413 (1988). 21 ancestors in all, the oldest K801623 (1980). 1 later device descends from it, 1 citing it directly.

  1. Root · 9 generations backK884413 Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc. · 1988
  2. 5 generations between
  3. 3 generations backK182809 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2018 · Recalled
  4. 2 generations backK200774 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2020
  5. 1 generation backK221235 neXus Ultrasonic Surgical Aspirator SystemMisonix, Inc. · 2022
  6. This deviceK231117 neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC, A Bioventus Company · 2023
  7. Descendant · cites it directly · 0 of its ownK261448 neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC · 2026
Show all 9 generations
  1. Root · 9 generations backK884413 Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc. · 1988
  2. 8 generations backK981262 Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc. · 1998 · Recalled
  3. 7 generations backK021989 Selector Integra Ultrasonic Surgical Aspirator, Model OM 1530000M3Integra Neurosciences · 2002 · Recalled
  4. 6 generations backK042277 Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd. · 2004
  5. 5 generations backK081459 Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc. · 2008 · Recalled
  6. 4 generations backK161882 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2016 · Recalled
  7. 3 generations backK182809 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2018 · Recalled
  8. 2 generations backK200774 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2020
  9. 1 generation backK221235 neXus Ultrasonic Surgical Aspirator SystemMisonix, Inc. · 2022
  10. This deviceK231117 neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC, A Bioventus Company · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K884413Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc.1988—
−8K981262Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc.19983
−7K021989Selector Integra Ultrasonic Surgical Aspirator, Model OM 1530000M3Integra Neurosciences20022
−6K042277Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd.2004—
−5K081459Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc.20084
−4K161882CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation20162
−3K182809CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation201842
−2K200774CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation2020—
−1K221235neXus Ultrasonic Surgical Aspirator SystemMisonix, Inc.2022—
0 (this device)K231117neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC, A Bioventus Company2023—
+1K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199010
199210
199310
199410
199510
200120
200210
200510
200710
201410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K231117, 1988–2026Source: 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 LFL? 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 LFL device

  1. #1 K261448 neXus Ultrasonic Surgical Aspirator Systemscore 14.5 · 10 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
*K221235neXus Ultrasonic Surgical Aspirator System
Summary page 7
…ct Code: LFL, GEI 3. PREDICATE DEVICE Predicate Device: neXus Ultrasonic Aspirator System with SonaStar Elite Handpiece (K221235) The predicate device has not been subject to a design-related recall. 4. DEVICE DESCRIPTION The neXus Ultrasonic Surgi…
Misonix, Inc.2022—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLC20260

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 35 years and passes through 7 companies; a new generation was cleared every 2.1 years on median.
  • 7 of the 21 ancestors have a recall of any class.
  • Of its descendants, K261448 (Misonix, LLC, 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LFL devices

LFL Instrument, Ultrasonic Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · LFL

3in 2025

2007: 72008: 22009: 12010: 22011: 32012: 32013: 52014: 32015: 42016: 52017: 22018: 32019: 42020: 42021: 62022: 82023: 42024: 32025: 32026 (partial year): 3
2007high 8 (2022) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LFL

176in 2025

2007: 99 days median2011: 241 days median2012: 82 days median2013: 73 days median2014: 136 days median2015: 99 days median2016: 111 days median2018: 66 days median2019: 103 days median2020: 190 days median2021: 83 days median2022: 168 days median2023: 104 days median2024: 158 days median2025: 176 days median2026 (partial year): 99 days median
2007high 241 (2011) · low 66 (2018)2026

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

Recalls per year · LFL

11in 2024

2010: 32011: 22012: 52014: 12015: 12017: 12019: 422021: 12023: 22024: 112026 (partial year): 1
2007high 42 (2019) · low 0 (2007)2026

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

Adverse event reports per year · LFL

3,857in 2025

2007: 2,2362008: 1,6782009: 3,3242010: 1,2392011: 1,0532012: 1,4912013: 2,4302014: 4,2602015: 2,7772016: 2,6912017: 3,2672018: 3,4612019: 3,1532020: 2,9342021: 3,2892022: 3,4222023: 4,2152024: 4,0172025: 3,857
2007high 4,260 (2014) · low 1,053 (2011)2025

MAUDE reports naming product code LFL, 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
200779902,236
20082—01,678
20091—03,324
20102—31,239
2011324121,053
201238251,491
201357302,430
2014313614,260
201549912,777
2016511102,691
20172—13,267
201836603,461
20194103423,153
2020419002,934
202168313,289
2022816803,422
2023410424,215
20243158114,017
2025317603,857
20263991—

What is it indicated for?

The Misonix Inc. neXus® Ultrasonic Surgical Aspirator System is intended for the fragmentation, emulsification and aspiration of both soft and hard (i.e., bone) tissue. The indications for use for the Standard Handpiece in combination with BoneScalpel® and SonicOne® OR probe kit accessory configurations, the SonaStar® Long and Short handpieces in combination with SonaStar® probe kit accessory configurations, the BoneScalpel Access® handpiece with…

Read the full statement (867 words)

The Misonix Inc. neXus® Ultrasonic Surgical Aspirator System is intended for the fragmentation, emulsification and aspiration of both soft and hard (i.e., bone) tissue.

The indications for use for the Standard Handpiece in combination with BoneScalpel® and SonicOne® OR probe kit accessory configurations, the SonaStar® Long and Short handpieces in combination with SonaStar® probe kit accessory configurations, the BoneScalpel Access® handpiece with BoneScalpel Access® probe kit accessory configurations, and the SonaStar Elite Handpiece with probe kit accessory configurations are listed below.

Standard Handpiece with BoneScalpel Probe Kit

Indicated for use in the fragmentation, emulsification and aspiration of soft and hard (e.g., bone) tissue in the following surgical specialties:

• Neurosurgery

• Gastrointestinal and Affiliated Organ Surgery

• Urological Surgery

• Plastic and Reconstructive Surgery

• General Surgery

• Orthopedic Surgery

• Gynecology

External genitalia - condyloma - benign tumors (lipomas, fibromas, and leiomyomas) - malignant primary and metastatic tumors of all types and the following cystic lesions: Bartholin's cysts, Vestibular adenitis, Inclusion cysts, Sebaceous cysts

Abdominal area - any abnormal growth, cystic or solid, benign or malignant, involving the ovary, fallopian tube, uterus, or the supporting structures of the uterus except as contraindicated for uterine fibroids.

• Thoracic Surgery

Limited pulmonary resection such as segmentectomies, nonanatomical subsegmentectomies and metastatectomies.

• Wound Care

The neXus Ultrasonic Surgical Aspirator is also indicated for use in the debridement of wounds, such as, but not limited to, burn wounds, diabetic ulcers, bedsores and vaginal ulcers, soft tissue debridement and cleansing of the surgical site in applications in which, in the physician's judgment would require the use of an ultrasonic aspirator with sharp debridement.

Standard Handpiece with SonicOne Probe Kits

Indicated for use in the fragmentation, emulsification and aspiration of soft and hard tissue (i.e. bone) in the following surgical specialty:

• Wound Care

The neXus Ultrasonic Surgical Aspirator is also indicated for use in the debridement of wounds, such as, but not limited to, burn wounds, diabetic ulcers, bedsores and vaginal ulcers, soft tissue debridement and cleansing of the surgical site in applications in which, in the physician's judgment would require the use of an ultrasonic aspirator with sharp debridement.

• Plastic and Reconstructive Surgery

neXus SonaStar Handpieces with SonaStar Probe Kits

Indicated for use in the fragmentation, emulsification and aspiration of both soft and hard (i.e., bone) tissue in the following surgical specialties:

• Neurosurgery

• Gastrointestinal and Affiliated Organ Surgery – including removal of benign or malignant tumors or other unwanted tissue, including hepatic parenchyma, in open or laparoscopic procedures, hepatic resection, tumor resection, lobectomy or trisegmentectomy, or removal of tissue during liver allotransplantation and donor hepatectomy

• Urological Surgery - including removal of renal parenchyma during nephrectomy or partial nephrectomy

• Plastic and Reconstructive Surgery

• General Surgery - including removal of benign or malignant tumors or other unwanted tissue in open or minimally invasive general surgical procedures

• Orthopedic Surgery

• Gynecological Surgery – except as contraindicated for uterine fibroids.

• Thoracic Surgery

• Laparoscopic Surgery – including removal of hepatic parenchyma in laparoscopic hepatic resection, lobectomy or trisegmentectomy, in laparoscopic donor hepatectomy or laparoscopic cholecystectomy or laparoscopic pancreatic jejunostomy, or pancreatectomy, or laparoscopic appendectomy, laparoscopic colon resection or laparoscopic partial gastrectomy

• Thoracoscopic Surgery

The SonaStar Handpieces may also be combined with electrosurgery using optional RF surgery interface components.

Bone Scalpel Access Handpiece with BoneScalpel Access Probe Kits

Indicated for use in the fragmentation and aspiration of soft and hard (e.g., bone) tissue in the following surgical specialties:

• Neurosurgery

• Gastrointestinal and Affiliated Organ Surgery

• Urological Surgery

• Plastic and Reconstructive Surgery

• General Surgery

• Orthopedic Surgery

• Gynecology

External genitalia - condyloma - benign tumors (lipomas, fibromas, and leiomyomas) - malignant primary and metastatic tumors of all types and the following cystic lesions: Bartholin's cysts, Vestibular adenitis, Inclusion cysts, Sebaceous cysts

Abdominal area - any abnormal growth, cystic or solid, benign or malignant, involving the ovary, fallopian tube, uterus, or the supporting structures of the uterus except as contraindicated for uterine fibroids.

• Thoracic Surgery

Limited pulmonary resection such as segmentectomies, nonanatomical subsegmentectomies and metastatectomies.

SonaStar Elite Handpiece with SonaStar Elite Probe Kits

Indicated for use in the fragmentation and aspiration of soft and hard (e.g., bone) tissue in the following surgical specialties:

• Neurosurgery

• Gastrointestinal and Affiliated Organ Surgery – including removal of benign or malignant tumors or other unwanted tissue, including hepatic parenchyma, in open or laparoscopic procedures, hepatic resection, tumor resection, lobectomy or trisegmentectomy, or removal of tissue during liver allotransplantation and donor hepatectomy

• Urological Surgery - including removal of renal parenchyma during nephrectomy or partial nephrectomy

• Plastic and Reconstructive Surgery

• General Surgery - including removal of benign or malignant tumors or other unwanted tissue in open or minimally invasive general surgical procedures

• Orthopedic Surgery

• Gynecological Surgery – except as contraindicated for uterine fibroids.

• Thoracic Surgery

• Laparoscopic Surgery – including removal of hepatic parenchyma in laparoscopic hepatic resection, lobectomy or trisegmentectomy, in laparoscopic donor hepatectomy or laparoscopic cholecystectomy or laparoscopic pancreatic jejunostomy, or pancreatectomy, or laparoscopic appendectomy, laparoscopic colon resection or laparoscopic partial gastrectomy

• Thoracoscopic Surgery

The system may also be combined with electrosurgery using optional RF surgery interface components.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K231117: neXus Ultrasonic Surgical Aspirator System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K231117

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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