510(k) Report

510(k) · Cleared

Cleared

PowerX Lipo System

K190555510(k) SpecialCleared May 1, 201957-day reviewClass II21 CFR 878.5040

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

Solta Medical · QPB System, Suction, Lipoplasty For Removal

Cleared on May 1, 2019 as substantially equivalent to K110255 (Sound Surgical Technologies, LLC, 2011) after a 57-day review. Its family tree reaches back 2 generations to 2001.

Decided
May 1, 2019
Review
57 days
Class
Class II
Product code
QPB
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K012236 (2001). No later device cites it as a predicate yet.

  1. Root · 2 generations backK012236 STARS2000 Power CannulaKmi Kolster Methods, Inc. · 2001
  2. 1 generation backK110255 Sound Surgical Technologies LLC Powerx Lipo SystemSound Surgical Technologies, LLC · 2011
  3. This deviceK190555 PowerX Lipo SystemSolta Medical · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K012236STARS2000 Power CannulaKmi Kolster Methods, Inc.2001—
−1K110255Sound Surgical Technologies LLC Powerx Lipo SystemSound Surgical Technologies, LLC2011—
0 (this device)K190555PowerX Lipo SystemSolta Medical2019—
FIG. 1 — Lineage of K190555, 2001–2019Source: 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 QPB? 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 QPB device

  1. #1 K212024 PAL Systemscore 13.7 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K110255Sound Surgical Technologies LLC Powerx Lipo System
Summary page 5
…: 21 CFR 878.5040 Product Codes: MUU Performance Standards: No performance standards for this device. 3. Predicate Device K110255 PowerX Lipo System 4. Product Description The subject of this Special 510(k) submission is for the PowerX Lipo System which…
Sound Surgical Technologies, LLC2011—

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 18 years and passes through 3 companies; a new generation was cleared every 9.4 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All QPB devices

QPB System, Suction, Lipoplasty For Removal: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · QPB

5so far in 2026, the most since 2007

2007: 22008: 42009: 12010: 22011: 22012: 32014: 12015: 12016: 12017: 32019: 22020: 22022: 22024: 42025: 22026 (partial year): 5
2007high 5 (2026) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · QPB

194in 2024

2008: 69 days median2012: 234 days median2017: 112 days median2024: 194 days median2026 (partial year): 238 days median
2007high 238 (2026) · low 69 (2008)2026

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

Recalls per year · QPB

No recall names QPB since 2007.

Adverse event reports per year · QPB

16in 2025

2022: 52023: 282024: 162025: 16
2007high 28 (2023) · low 0 (2007)2025

MAUDE reports naming product code QPB, 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
20072—00
200846900
20091—00
20102—00
20112—00
2012323400
20130—00
20141—00
20151—00
20161—00
2017311200
20180—00
20192—00
20202—00
20210—00
20222—05
20230—028
20244194016
20252—016
202652380—

What is it indicated for?

The PowerX Lipo System is intended for the removal of tissues or fluids from the body during general surgical procedures including suction lipoplasty for the purpose of aesthetic body contouring.

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. “K190555: PowerX Lipo System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K190555

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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