510(k) Report

510(k) · Cleared

Cleared

Vitruvian Infiltration Pump

K170629510(k) TraditionalCleared Jun 22, 2017112-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

Black & Black Surgical, Inc. · QPB System, Suction, Lipoplasty For Removal

Cleared on Jun 22, 2017 as substantially equivalent to K031432 (Hk Surgical, Inc., 2003) and 1 other predicate after a 112-day review. Its family tree reaches back 6 generations to 1989. 1 later device descends from it.

Decided
Jun 22, 2017
Review
112 days
Class
Class II
Product code
QPB
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K895761 (1989). 12 ancestors in all, the oldest K832274 (1983). 1 later device descends from it, 1 citing it directly.

  1. Root · 6 generations backK895761 General AsperatorKolster Methods · 1989
  2. 5 generations backK980392 Psi-Tec AspiratorByron Medical · 1998
  3. 4 generations backK981215 Psi-Tec Liposuction AspiratorByron Medical · 1998
  4. 3 generations backK032802 HK Liposuction Aspirator, Model AP-Iii & AP230-IiiHk Surgical, Inc. · 2003
  5. 2 generations backK053451 Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction…Moeller Medical GmbH & Co. KG · 2006
  6. 1 generation backK072793 Liposat Basic (Infiltration Pump), Model 92-007 688Moeller Medical GmbH & Co. KG · 2008
  7. This deviceK170629 Vitruvian Infiltration PumpBlack & Black Surgical, Inc. · 2017
  8. Descendant · cites it directly · 0 of its ownK220318 PAL Infiltration SystemMicroaire Surgical Instruments, LLC · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K220318PAL Infiltration SystemMicroaire Surgical Instruments, LLC · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K895761General AsperatorKolster Methods1989—
−5K980392Psi-Tec AspiratorByron Medical1998—
−4K981215Psi-Tec Liposuction AspiratorByron Medical1998—
−3K032802HK Liposuction Aspirator, Model AP-Iii & AP230-IiiHk Surgical, Inc.2003—
−2K053451Liposat (Infiltration Pump), Model 00 002 274; Vacusat (Suction Unit), Model…Moeller Medical GmbH & Co. KG2006—
−1K072793Liposat Basic (Infiltration Pump), Model 92-007 688Moeller Medical GmbH & Co. KG2008—
0 (this device)K170629Vitruvian Infiltration PumpBlack & Black Surgical, Inc.2017—
+1K220318PAL Infiltration SystemMicroaire Surgical Instruments, LLC2022—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198310
198610
199820
200010
200310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K170629, 1989–2022Source: 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
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
*K031432Klein Surgical Infiltration Pump, Model Kip-II
Summary page 5
…infiltration devices listed below in terms of use, design, operating principles, materials and performance. HK Surgical: K031432 MOELLER MEDICAL GMBH & CO. KG: K072793 6. Device Description: The B89055 Vitruvian Infiltrati…
Hk Surgical, Inc.2003—
*K072793Liposat Basic (Infiltration Pump), Model 92-007 688
Summary page 5
…operating principles, materials and performance. HK Surgical: K031432 MOELLER MEDICAL GMBH & CO. KG: K072793 6. Device Description: The B89055 Vitruvian Infiltration Pump is intended to be used for aesthetic body contouring.…
Moeller Medical GmbH & Co. KG2008—

Also cleared against K031432: 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
K220318PAL Infiltration SystemMicroaire Surgical Instruments, LLC20220

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 28 years and passes through 5 companies; a new generation was cleared every 5.4 years on median.
  • None of the 12 ancestors has a recall.
  • Of its descendants, K220318 (Microaire Surgical Instruments, LLC, 2022) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K031432.

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. 2017, 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?

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. “K170629: Vitruvian Infiltration Pump.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K170629

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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