510(k) · Cleared

Cleared

Penevac Abc Handpiece

K955020510(k) TraditionalCleared Apr 9, 1996159-day reviewClass II21 CFR 878.4400

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

I.C Medical, Inc. · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Apr 9, 1996 as substantially equivalent to K954088 (I.C Medical, Inc., 1995) after a 159-day review. Its family tree reaches back 1 generation to 1995. 1 later device descends from it.

Decided: Apr 9, 1996
Review: 159 days
Class: Class II
Product code: GEI
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K954088 (1995). 1 later device descends from it, 1 citing it directly.

By dateBy generation

Root · 1 generation backK954088 Telescoping PenevacI.C Medical, Inc. · 1995
This deviceK955020 Penevac Abc HandpieceI.C Medical, Inc. · 1996
Descendant · cites it directly · 0 of its ownK113500 Canady Vieira Hybrid Plasma ScalpelUs Medical Innovations, LLC · 2011

Most influential descendants

Showing 1 of 1 · See all

K113500Canady Vieira Hybrid Plasma ScalpelUs Medical Innovations, LLC · 2011 · cites it directly0descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K954088	Telescoping Penevac	I.C Medical, Inc.	1995	—
0 (this device)	K955020	Penevac Abc Handpiece	I.C Medical, Inc.	1996	—
+1	K113500	Canady Vieira Hybrid Plasma Scalpel	Us Medical Innovations, LLC	2011	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2011	1	0

FIG. 1 — Lineage of K955020, 1995–2011Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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 GEI? 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 GEI device

#1 K231790 The InMode System with the Morpheus8 Applicatorsscore 32.7 · 21 generations · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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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.

Type	Number	Device	Applicant	Decided	Recalls
*	K954088	Telescoping Penevac Summary page 2 …handswitching pencil, and an argon beam coagulator handpiece. The smoke evacuator and electrosurgery portions are being compared to the I.C. Medical Telescoping PenEvac (K954088) and the argon beam coagulator handpiece portion is being compared to the ValleyLab Force GSU Handset (catalog number E2522H). Th…	I.C Medical, Inc.	1995	—
*	—	Valleylab Force GSU Handset Named without a submission number			—

Also cleared against K954088: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K113500	Canady Vieira Hybrid Plasma Scalpel	Us Medical Innovations, LLC	2011	0

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?

Its one ancestor has no recall.
Of its descendants, K113500 (Us Medical Innovations, LLC, 2011) has gone furthest, with 0 descendants of its own.
2 other devices also cite its predicate K954088.

How does its category compare?

All GEI devices

GEI Electrosurgical, Cutting & Coagulation & Accessories: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GEI

52in 2025

2007high 65 (2023) · low 35 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GEI

113in 2025

2007high 183 (2026) · low 51 (2007)2026

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

Recalls per year · GEI

4in 2025

2007high 51 (2010) · low 1 (2020)2026

Class I (14 since 2007) Class II/III not classified

Adverse event reports per year · GEI

7,592in 2025

2007high 7,897 (2024) · low 2,556 (2008)2025

MAUDE reports naming product code GEI, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	50	51	21	2,795
2008	61	71	19	2,556
2009	42	130	27	3,591
2010	46	109	51	3,377
2011	35	135	32	4,463
2012	39	133	30	5,216
2013	48	136	13	4,897
2014	49	103	3	4,908
2015	47	123	4	4,936
2016	64	108	3	5,616
2017	52	72	2	6,073
2018	47	93	6	6,545
2019	48	93	5	7,067
2020	59	105	1	6,490
2021	46	146	6	6,354
2022	55	150	49	6,103
2023	65	104	27 (4)	7,176
2024	59	125	22 (10)	7,897
2025	52	113	4	7,592
2026	43	183	8	—

What is it indicated for?

The Telescoping PenEvac ABC is intended to be used only during open surgical procedures as the active handpiece in a combination argon beam coagulator/electrosurgery generator system that uses monopolar electrodes and to facilitate the removal of smoke that is generated.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

https://510kreport.com/device/K955020 · printed Nov 5, 2026

Cite this page

510(k) Report. “K955020: Penevac Abc Handpiece.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K955020

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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