510(k) Report

510(k) · Cleared

Cleared

CUSA Clarity Ultrasonic Surgical Aspirator System

K190180510(k) TraditionalCleared Apr 1, 201959-day reviewClass U

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

Integra LifeSciences Corporation · LFL Instrument, Ultrasonic Surgical

Cleared on Apr 1, 2019 as substantially equivalent to K141668 (Integra LifeSciences Corporation, 2014) and 1 other predicate after a 59-day review. Its family tree reaches back 7 generations to 1988. 1 later device descends from it.

Decided
Apr 1, 2019
Review
59 days
Class
Class U
Product code
LFL
Recalls
None
Predicates
2

Its longest line of descent runs back 7 generations to K884413 (1988). 19 ancestors in all, the oldest K801623 (1980). 1 later device descends from it, 1 citing it directly.

  1. Root · 7 generations backK884413 Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc. · 1988
  2. 6 generations backK981262 Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc. · 1998 · Recalled
  3. 5 generations backK021989 Selector Integra Ultrasonic Surgical Aspirator, Model OM 1530000M3Integra Neurosciences · 2002 · Recalled
  4. 4 generations backK042277 Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd. · 2004
  5. 3 generations backK081459 Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc. · 2008 · Recalled
  6. 2 generations backK161882 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2016 · Recalled
  7. 1 generation backK182809 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2018 · Recalled
  8. This deviceK190180 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2019
  9. Descendant · cites it directly · 0 of its ownK230427 CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K230427CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K884413Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc.1988—
−6K981262Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc.19983
−5K021989Selector Integra Ultrasonic Surgical Aspirator, Model OM 1530000M3Integra Neurosciences20022
−4K042277Selector Quantum Ultrasonic Aspirator SystemIntegra Neurosciences, Ltd.2004—
−3K081459Cusa Selector NXT Ultrasonic Tissue Ablation SystemIntegra Radionics, Inc.20084
−2K161882CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation20162
−1K182809CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation201842
0 (this device)K190180CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation2019—
+1K230427CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation2023—

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
202310
FIG. 1 — Lineage of K190180, 1988–2023Source: 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 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? (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
*K141668Cusa Excel+ Ultrasonic Surgical Aspirator System
Summary page 4
…tion Unclassified Product Code(s) LFL, LBK 807.92(a)(3) - Legally marketed device(s) to which equivalence is claimed CUSA® Excel+ Ultrasonic Surgical Aspirator System K 141668 CUSA® Clarity Ultrasonic Surgical Aspirator System K 182809 K190180 Page 2 of 4 807.92(a)(4) - Device descriptio…
Integra LifeSciences Corporation2014—
*K182809CUSA Clarity Ultrasonic Surgical Aspirator System
Summary page 4
…Legally marketed device(s) to which equivalence is claimed CUSA® Excel+ Ultrasonic Surgical Aspirator System K 141668 CUSA® Clarity Ultrasonic Surgical Aspirator System K 182809 K190180 Page 2 of 4 807.92(a)(4) - Device description The device within the scope of this premarket notificatio…
Integra LifeSciences Corporation201842

Also cleared against K141668: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K230427CUSA Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation20230

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 31 years and passes through 5 companies; a new generation was cleared every 3.9 years on median.
  • 7 of the 19 ancestors have a recall of any class.
  • Of its descendants, K230427 (Integra LifeSciences Corporation, 2023) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K141668.

How does its category compare?

All LFL devices

LFL Instrument, Ultrasonic Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, 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 CUSA® Clarity Ultrasonic Surgical Aspirator System is indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard (e.g. bone) tissue is desirable. The CUSA Clarity Ultrasonic Surgical Aspirator is indicated for use in: Neurosurgery, Plastic and Reconstructive surgery, Orthopedic Surgery, Gynecological Surgery and Thoracic Surgery and the following specific uses: Gastrointestinal and Affiliated Organ…

Read the full statement (171 words)

The CUSA® Clarity Ultrasonic Surgical Aspirator System is indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard (e.g. bone) tissue is desirable.

The CUSA Clarity Ultrasonic Surgical Aspirator is indicated for use in:

Neurosurgery, Plastic and Reconstructive surgery, Orthopedic Surgery, Gynecological Surgery and Thoracic Surgery and the following specific uses:

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

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

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

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K190180: CUSA Clarity Ultrasonic Surgical Aspirator System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K190180

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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