510(k) Report

510(k) · Cleared

Cleared

Avance Tubing, Avance Y-Connector, Avance ViewPad

K161797510(k) TraditionalCleared Oct 19, 2016111-day reviewClass II21 CFR 878.4780

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

Molnlycke Health Care Us, LLC · OMP Negative Pressure Wound Therapy Powered Suction Pump

Cleared on Oct 19, 2016 as substantially equivalent to K080897 (Talley Medical, 2008) and 2 other predicates after a 111-day review. Its family tree reaches back 9 generations to 1995.

Decided
Oct 19, 2016
Review
111 days
Class
Class II
Product code
OMP
Recalls
None
Predicates
3

Its longest line of descent runs back 9 generations to K945062 (1995). 26 ancestors in all, the oldest K914604 (1992). No later device cites it as a predicate yet.

  1. Root · 9 generations backK945062 VacplusKinetic Concepts, Inc. · 1995
  2. 5 generations between
  3. 3 generations backK122132 Avance Foam Dressing Kit Incl. Transparent Film, Transfer Pad…Molnlycke Health Care · 2013
  4. 2 generations backK141847 Avance Foam Dressing KitsMolnlycke Health Care Us, LLC · 2015
  5. 1 generation backK151872 Avance Y-Connector SMolnlycke Health Care Us, LLC · 2015
  6. This deviceK161797 Avance Tubing, Avance Y-Connector, Avance ViewPadMolnlycke Health Care Us, LLC · 2016
Show all 9 generations
  1. Root · 9 generations backK945062 VacplusKinetic Concepts, Inc. · 1995
  2. 8 generations backK042134 Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2004 · Recalled
  3. 7 generations backK052456 Modification to Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2005
  4. 6 generations backK061919 Versatile 1 Ezcare Wound Vacuum SystemBlue Sky Medical Group Incorporated · 2007 · Recalled
  5. 5 generations backK082211 Renasys-F Negative Pressure Wound Therapy Foam Dressing KitsSmith & Nephew, Inc. · 2008 · Recalled
  6. 4 generations backK110647 Renasys Foam NPWT Wound Dressing Kits with Suction Pad; Renasys…Smith & Nephew, Inc. · 2011 · Recalled
  7. 3 generations backK122132 Avance Foam Dressing Kit Incl. Transparent Film, Transfer Pad…Molnlycke Health Care · 2013
  8. 2 generations backK141847 Avance Foam Dressing KitsMolnlycke Health Care Us, LLC · 2015
  9. 1 generation backK151872 Avance Y-Connector SMolnlycke Health Care Us, LLC · 2015
  10. This deviceK161797 Avance Tubing, Avance Y-Connector, Avance ViewPadMolnlycke Health Care Us, LLC · 2016
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K945062VacplusKinetic Concepts, Inc.1995—
−8K042134Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated20042
−7K052456Modification to Versatile 1 Wound Vacuum SystemBlue Sky Medical Group Incorporated2005—
−6K061919Versatile 1 Ezcare Wound Vacuum SystemBlue Sky Medical Group Incorporated20071
−5K082211Renasys-F Negative Pressure Wound Therapy Foam Dressing KitsSmith & Nephew, Inc.20081
−4K110647Renasys Foam NPWT Wound Dressing Kits with Suction Pad; Renasys Gauze NPWT…Smith & Nephew, Inc.20116
−3K122132Avance Foam Dressing Kit Incl. Transparent Film, Transfer Pad (Small, Medium…Molnlycke Health Care2013—
−2K141847Avance Foam Dressing KitsMolnlycke Health Care Us, LLC2015—
−1K151872Avance Y-Connector SMolnlycke Health Care Us, LLC2015—
0 (this device)K161797Avance Tubing, Avance Y-Connector, Avance ViewPadMolnlycke Health Care Us, LLC2016—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199410
199710
199920
200010
200210
200310
200510
200640
200710
200820
201510
FIG. 1 — Lineage of K161797, 1995–2016Source: 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 OMP? 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 OMP device

  1. #1 K260646 Renasys Edge (66803126)score 15.3 · 14 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? (3)

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
*K080897Venturi Negative Pressure Wound Therapy System
Summary page 4
…21 CFR 878.4780 Product Code: OMP Predicate Device Information: Venturi Negative Pressure Wound Therapy System (K080897) Avance® Y-Connector S (K151872) Avance® Foam…
Talley Medical2008—
*K151872Avance Y-Connector S
Summary page 4
…OMP Predicate Device Information: Venturi Negative Pressure Wound Therapy System (K080897) Avance® Y-Connector S (K151872) Avance® Foam Dressing Kits (K141847) Reason for 510(k) Submission: This premarket not…
Molnlycke Health Care Us, LLC2015—
*K141847Avance Foam Dressing Kits
Summary page 4
…Therapy System (K080897) Avance® Y-Connector S (K151872) Avance® Foam Dressing Kits (K141847) Reason for 510(k) Submission: This premarket notification has been prepared to obtain clearance for the following line addition…
Molnlycke Health Care Us, LLC2015—

Also cleared against K080897: 2 other devices →

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 21 years and passes through 5 companies; a new generation was cleared every 1.6 years on median.
  • 9 of the 26 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K080897.

How does its category compare?

All OMP devices

OMP Negative Pressure Wound Therapy Powered Suction Pump: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · OMP

5in 2025

2007: 62008: 82009: 82010: 62011: 62012: 112013: 112014: 102015: 202016: 192017: 112018: 132019: 152020: 62021: 92022: 102023: 82024: 92025: 52026 (partial year): 9
2007high 20 (2015) · low 5 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OMP

127in 2025

2007: 113 days median2008: 98 days median2009: 87 days median2010: 97 days median2011: 123 days median2012: 292 days median2013: 84 days median2014: 179 days median2015: 189 days median2016: 146 days median2017: 137 days median2018: 214 days median2019: 249 days median2020: 179 days median2021: 238 days median2022: 229 days median2023: 291 days median2024: 181 days median2025: 127 days median2026 (partial year): 141 days median
2007high 292 (2012) · low 84 (2013)2026

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

Recalls per year · OMP

2in 2024

2009: 72010: 32012: 12013: 22014: 42015: 12016: 22019: 12024: 2
2007high 7 (2009) · low 0 (2007)2026

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

Adverse event reports per year · OMP

140in 2025

2007: 12008: 12009: 792010: 802011: 1302012: 972013: 1692014: 2292015: 3782016: 3982017: 3682018: 4222019: 9942020: 3,6642021: 1,4222022: 2582023: 1432024: 1352025: 140
2007high 3,664 (2020) · low 1 (2007)2025

MAUDE reports naming product code OMP, 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
2007611301
200889801
2009887779
2010697380
201161230130
201211292197
201311842169
2014101794229
2015201891378
2016191462398
2017111370368
2018132140422
2019152491994
2020617903,664
2021923801,422
2022102290258
202382910143
202491812135
202551270140
202691410—

What is it indicated for?

The Avance NPWT system, with associated products, are indicated for patients who would benefit from a suction device (negative pressure wound therapy), as it may promote wound healing via the removal of fluids, including irrigation and body fluids, wound exudate and infectious materials. Examples of appropriate wound types include: chronic, acute, traumatic, sub-acute and dehisced wounds, ulcers (such as pressure or diabetic), partial-thickness bums, flaps and grafts.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K161797: Avance Tubing, Avance Y-Connector, Avance ViewPad.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K161797

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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