510(k) Report

510(k) · Cleared

Cleared

PK Lap Loop

K142525510(k) TraditionalCleared Nov 21, 201474-day reviewClass II21 CFR 884.4150

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

Olympus Winter & Ibe GmbH · HIN Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)

Cleared on Nov 21, 2014 as substantially equivalent to K122605 (Gyrus Acmi, Inc., 2012) and 1 other predicate after a 74-day review. Its family tree reaches back 12 generations to 1994.

Decided
Nov 21, 2014
Review
74 days
Class
Class II
Product code
HIN
Recalls
None
Predicates
2

Its longest line of descent runs back 12 generations to K936109 (1994). 81 ancestors in all, the oldest K800617 (1980). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2007: 1 other ancestor2004: 1 other ancestor2005: 1 other ancestor2003: 3 other ancestors2000: 13 other ancestors1998: 7 other ancestors2002: 2 other ancestors2001: 4 other ancestors1997: 4 other ancestors1991: 4 other ancestors1985: 1 other ancestor1996: 8 other ancestors1995: 7 other ancestors1994: 4 other ancestors1992: 3 other ancestors1999: 1 other ancestor1980: 1 other ancestor1993: 1 other ancestor1990: 1 other ancestor1989: 1 other ancestor1986: 1 other ancestorK936109 · Sharplan Model 1120 CO2 Surgical Laser · Sharplan Lasers, Inc. · 1994K960521 · Sharplan Lasers, Inc. Silktouch Flash Scanner · Sharplan Lasers, Inc. · 1996K963339 · Coherent Ultrapulse CO2 Surgical Lasers · Coherent Medical Group · 1997K974789 · Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and L · Lumenis, Inc. · 1998K990947 · Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO: Yag/ND: Yag Surgical Lasers and Delivery · Lumenis, Inc. · 1999K011703 · Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength (HO:Yag/ND:Yag) Surgical Lasers and Delivery Devices · Lumenis · 2001 · recalledK014290 · Entec Plasma Wands · Arthrocare Corp. · 2002K021777 · Gyrus Ent Cogent 2/G2 System (Generator,Accessories Somnoplasty Electrodes and Plasmacision Electrodes) · Gyrus Ent LLC · 2002K041285 · Gyrus G3 System (Generator, Assessories, Somnoplasty Electrodes and Plasmacision Electrodes) · Gyrus Medical, Ltd. · 2004 · recalledK050550 · Gyrus General Purpose Electrosurgical Generator · Gyrus Medical, Inc. · 2005K111059 · Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill) · Gyrus Acmi, Inc. · 2011K122605 · PKS Bill · Gyrus Acmi, Inc. · 201219801985199019952000200520102015
Other ancestors, by generation 2 generations back: 2 other ancestors3 generations back: 6 other ancestors4 generations back: 16 other ancestors5 generations back: 16 other ancestors6 generations back: 9 other ancestors7 generations back: 11 other ancestors8 generations back: 5 other ancestors9 generations back: 3 other ancestors10 generations back: 1 other ancestor K122605 · PKS Bill · Gyrus Acmi, Inc. · 2012K111059 · Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill) · Gyrus Acmi, Inc. · 2011K050550 · Gyrus General Purpose Electrosurgical Generator · Gyrus Medical, Inc. · 2005K041285 · Gyrus G3 System (Generator, Assessories, Somnoplasty Electrodes and Plasmacision Electrodes) · Gyrus Medical, Ltd. · 2004 · recalledK021777 · Gyrus Ent Cogent 2/G2 System (Generator,Accessories Somnoplasty Electrodes and Plasmacision Electrodes) · Gyrus Ent LLC · 2002K014290 · Entec Plasma Wands · Arthrocare Corp. · 2002K011703 · Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength (HO:Yag/ND:Yag) Surgical Lasers and Delivery Devices · Lumenis · 2001 · recalledK990947 · Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO: Yag/ND: Yag Surgical Lasers and Delivery · Lumenis, Inc. · 1999K974789 · Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and L · Lumenis, Inc. · 1998K963339 · Coherent Ultrapulse CO2 Surgical Lasers · Coherent Medical Group · 1997K960521 · Sharplan Lasers, Inc. Silktouch Flash Scanner · Sharplan Lasers, Inc. · 1996K936109 · Sharplan Model 1120 CO2 Surgical Laser · Sharplan Lasers, Inc. · 1994−10−50
  1. Root · 12 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
  2. 8 generations between
  3. 3 generations backK050550 Gyrus General Purpose Electrosurgical GeneratorGyrus Medical, Inc. · 2005
  4. 2 generations backK111059 Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill)Gyrus Acmi, Inc. · 2011
  5. 1 generation backK122605 PKS BillGyrus Acmi, Inc. · 2012
  6. This deviceK142525 PK Lap LoopOlympus Winter & Ibe GmbH · 2014
Show all 12 generations
  1. Root · 12 generations backK936109 Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc. · 1994
  2. 11 generations backK960521 Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc. · 1996
  3. 10 generations backK963339 Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group · 1997
  4. 9 generations backK974789 Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc. · 1998
  5. 8 generations backK990947 Modified Versapulse Select Single Wavelength, HO: Yag and Dual…Lumenis, Inc. · 1999
  6. 7 generations backK011703 Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength…Lumenis · 2001 · Recalled
  7. 6 generations backK014290 Entec Plasma WandsArthrocare Corp. · 2002
  8. 5 generations backK021777 Gyrus Ent Cogent 2/G2 System (Generator,Accessories Somnoplasty…Gyrus Ent LLC · 2002
  9. 4 generations backK041285 Gyrus G3 System (Generator, Assessories, Somnoplasty Electrodes and…Gyrus Medical, Ltd. · 2004 · Recalled
  10. 3 generations backK050550 Gyrus General Purpose Electrosurgical GeneratorGyrus Medical, Inc. · 2005
  11. 2 generations backK111059 Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill)Gyrus Acmi, Inc. · 2011
  12. 1 generation backK122605 PKS BillGyrus Acmi, Inc. · 2012
  13. This deviceK142525 PK Lap LoopOlympus Winter & Ibe GmbH · 2014
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K936109Sharplan Model 1120 CO2 Surgical LaserSharplan Lasers, Inc.1994—
−11K960521Sharplan Lasers, Inc. Silktouch Flash ScannerSharplan Lasers, Inc.1996—
−10K963339Coherent Ultrapulse CO2 Surgical LasersCoherent Medical Group1997—
−9K974789Coherent Ultrapulse S Series CO2 Surgical Lasers Model C and LLumenis, Inc.1998—
−8K990947Modified Versapulse Select Single Wavelength, HO: Yag and Dual Wavelength, HO…Lumenis, Inc.1999—
−7K011703Lumenis Versapulse Powersuite Holmium (HO:Yag) and Dual Wavelength…Lumenis20012
−6K014290Entec Plasma WandsArthrocare Corp.2002—
−5K021777Gyrus Ent Cogent 2/G2 System (Generator,Accessories Somnoplasty Electrodes and…Gyrus Ent LLC2002—
−4K041285Gyrus G3 System (Generator, Assessories, Somnoplasty Electrodes and…Gyrus Medical, Ltd.20042
−3K050550Gyrus General Purpose Electrosurgical GeneratorGyrus Medical, Inc.2005—
−2K111059Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill)Gyrus Acmi, Inc.2011—
−1K122605PKS BillGyrus Acmi, Inc.2012—
0 (this device)K142525PK Lap LoopOlympus Winter & Ibe GmbH2014—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198010
198510
198610
198910
199010
199140
199230
199310
199440
199570
199680
199740
199870
199910
2000130
200140
200220
200330
200410
200510
200710
FIG. 1 — Lineage of K142525, 1994–2014Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 HIN? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin 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
*K122605PKS Bill
Summary page 6
…Regulations Number: 21 CFR 884.4150 Regulatory class: Class II Product code: HIN Predicate device K122605: PKS BILL Description of device The Bipolar Laparoscopic Loop is a single use disposable high frequency RF bipolar accesso…
Gyrus Acmi, Inc.2012—
*K111059Gyrus Acmil Bipolarlaproscopic Loop (PKS Bill)
Summary page 9
…output waveforms and power levels as the FDA cleared Gyrus G400 electrosurgical generator, K081954.  Just like the predicates PKS Bill (K122605 and K111059) the Lap Loop contains device recognition. It ensures that the PK Lap Loop can only be connected to the Olympus…
Gyrus Acmi, Inc.2011—

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 20 years and passes through 10 companies; a new generation was cleared every 1.3 years on median.
  • 5 of the 81 ancestors have a recall of any class.

How does its category compare?

All HIN devices

HIN Coagulator-Cutter, Endoscopic, Bipolar (And Accessories): FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · HIN

1in 2014

2011: 22012: 22013: 22014: 1
2007high 2 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HIN

Too few HIN 510(k)s in any year since 2007 to give a median.

Recalls per year · HIN

No recall names HIN since 2007.

Adverse event reports per year · HIN

43in 2025

2009: 62010: 72011: 62012: 12013: 142014: 122015: 82016: 22017: 82018: 22019: 42020: 92021: 102022: 12023: 92024: 292025: 43
2007high 43 (2025) · low 0 (2007)2025

MAUDE reports naming product code HIN, 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
20070—00
20080—00
20090—06
20100—07
20112—06
20122—01
20132—014
20141—012
20150—08
20160—02
20170—08
20180—02
20190—04
20200—09
20210—010
20220—01
20230—09
20240—029
20250—043
20260—0—

What is it indicated for?

The Bipolar Laparoscopic Loop PK Lap Loop is a Smm bipolar electrosurgical device. The device is intended to be used for the amputation of the mobilised uterus during Laparoscopic Supracervical (Subtotal) Hysterectomy and the resection of devascularized subserosal pedunculated myomas. It is used in conjunction with the Olympus Electrosurgical Generator ESG-400.

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. “K142525: PK Lap Loop.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K142525

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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