510(k) Report

510(k) · Cleared

Cleared

Ultrasonic Surgical Aspirator System

K202299510(k) TraditionalCleared May 21, 2021281-day reviewClass U

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

Smtp Technology Co., Ltd. · LFL Instrument, Ultrasonic Surgical

Cleared on May 21, 2021 as substantially equivalent to K070313 (Misonix, Inc., 2007) and 1 other predicate after a 281-day review. Its family tree reaches back 4 generations to 1988. 1 later device descends from it.

Decided
May 21, 2021
Review
281 days
Class
Class U
Product code
LFL
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K884413 (1988). 12 ancestors in all, the oldest K801623 (1980). 1 later device descends from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 2 other ancestors4 generations back: 3 other ancestors 1 generation forward: 1 descendant K062471 · Ultrasonic Surgical Aspirator System, Model FS 1000 RF · Misonix, Inc. · 2006K051947 · Radionics Cusa Excel Ultrasonic Surgical Aspirator System with Bone · Radionics, A Division of Tyco Healthcare Group LP · 2005K981262 · Cusa Excel Ultrasonic Surgical Aspirator System · Valleylab, Inc. · 1998 · recalledK884413 · Cusa System 200H Ultrasonic Surgical Aspirator · Valleylab, Inc. · 19880
  1. Root · 4 generations backK884413 Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc. · 1988
  2. 3 generations backK981262 Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc. · 1998 · Recalled
  3. 2 generations backK051947 Radionics Cusa Excel Ultrasonic Surgical Aspirator System with BoneRadionics, A Division of Tyco Healthcare Group LP · 2005
  4. 1 generation backK062471 Ultrasonic Surgical Aspirator System, Model FS 1000 RFMisonix, Inc. · 2006
  5. This deviceK202299 Ultrasonic Surgical Aspirator SystemSmtp Technology Co., Ltd. · 2021
  6. Descendant · cites it directly · 0 of its ownK212750 Ultrasonic Surgical Aspirator System, Model: XD880BSmtp Technology Co., Ltd. · 2021

Most influential descendants

Showing 1 of 1 · See all
  • K212750Ultrasonic Surgical Aspirator System, Model: XD880BSmtp Technology Co., Ltd. · 2021 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K884413Cusa System 200H Ultrasonic Surgical AspiratorValleylab, Inc.1988—
−3K981262Cusa Excel Ultrasonic Surgical Aspirator SystemValleylab, Inc.19983
−2K051947Radionics Cusa Excel Ultrasonic Surgical Aspirator System with BoneRadionics, A Division of Tyco Healthcare Group LP2005—
−1K062471Ultrasonic Surgical Aspirator System, Model FS 1000 RFMisonix, Inc.2006—
0 (this device)K202299Ultrasonic Surgical Aspirator SystemSmtp Technology Co., Ltd.2021—
+1K212750Ultrasonic Surgical Aspirator System, Model: XD880BSmtp Technology Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
199210
199410
199510
200110
200210
200510
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202110
FIG. 1 — Lineage of K202299, 1988–2021Source: 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
*K070313Misonix, Inc., Auss-7 Ultrasonic Surgical Aspirator System
Summary page 5
…Name Manufacturer Primary Predicate Alliger Ultrasonic Surgical System K070313 Misonix Inc. Device Model AUSS-7 Secondary Pre…
Misonix, Inc.2007—
*K062471Ultrasonic Surgical Aspirator System, Model FS 1000 RF
Summary page 5
…sonix Inc. Device Model AUSS-7 Secondary Predicate FS 1000 RF Ultrasonic Surgical K062471 Misonix Inc. Device Aspirator System and Accessories…
Misonix, Inc.2006—
†K172464XD880A Ultrasonic Osteotomy Surgical SystemMorley Research Consortium2018—

Also cleared against K070313: 3 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
K212750Ultrasonic Surgical Aspirator System, Model: XD880BSmtp Technology Co., Ltd.20210

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 33 years and passes through 4 companies; a new generation was cleared every 9.6 years on median.
  • 2 of the 12 ancestors have a recall of any class.
  • Of its descendants, K212750 (Smtp Technology Co., Ltd., 2021) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K070313.

How does its category compare?

All LFL devices

LFL Instrument, Ultrasonic Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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 XD880B Ultrasonic Surgical Aspirator System is an ultrasonic surgical system consisting of handpieces and associated tips. The product is intended for the fragmentation, emulsification and aspiration of both soft and hard (i.e. bone and bone approximations) tissue, the intended use is as follows with different configurations:

» Neurosurgery

» Gastrointestinal and Affiliated Organ Surgery

* Urological surgery

» Plastic and Reconstructive surgery

* General Surgery

* Orthopedic Surgery

* Gynecological Surgery

* Thoracic Surgery

* Wound Care

* Laparoscopic Surgery

» Thoracoscopic Surgery

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. “K202299: 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/K202299

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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