510(k) · Cleared

Cleared

Cautery Protective Actuation System (CPAS)

K232407510(k) TraditionalCleared Oct 6, 202357-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

Safer Surgeries Medical Devices, LLC · GEI Electrosurgical, Cutting & Coagulation & Accessories

Cleared on Oct 6, 2023 as substantially equivalent to K092732 (Bio Protech, Inc., 2009) after a 57-day review. Its family tree reaches back 2 generations to 1990.

Decided: Oct 6, 2023
Review: 57 days
Class: Class II
Product code: GEI
Recalls: None
Predicates: 1

Its longest line of descent runs back 2 generations to K896626 (1990). No later device cites it as a predicate yet.

By dateBy generation

Root · 2 generations backK896626 Hand Controlled Electrosurgical PencilsConmedcorp · 1990
1 generation backK092732 Propencil Esu PencilBio Protech, Inc. · 2009
This deviceK232407 Cautery Protective Actuation System (CPAS)Safer Surgeries Medical Devices, LLC · 2023

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K896626	Hand Controlled Electrosurgical Pencils	Conmedcorp	1990	—
−1	K092732	Propencil Esu Pencil	Bio Protech, Inc.	2009	—
0 (this device)	K232407	Cautery Protective Actuation System (CPAS)	Safer Surgeries Medical Devices, LLC	2023	—

FIG. 1 — Lineage of K232407, 1990–2023Source: 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

Get a 510(k) Report

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.

Type	Number	Device	Applicant	Decided	Recalls
*	K092732	Propencil Esu Pencil Summary page 5 …PAS) Common Name Electrocautery Pencil GXN Code –Classification 21 CFR 878.4400: Class II Primary Predicate K092732 Bio Protech, Inc Propencil ESU Pencil Device Description The Cautery Protective Actuation System device is a sterile, single-…	Bio Protech, Inc.	2009	—

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 33 years and passes through 3 companies; a new generation was cleared every 19.9 years on median.
None of the 2 ancestors has a recall.

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. 2023, this device’s year, is highlighted.

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 Cautery Protective Actuation System (CPAS) is intended for use in general surgical procedures to deliver electrosurgical energy to the surgery site for tissue cutting and coagulation. The CPAS device includes a safety cover intended to prevent inadvertent actuation of the monopolar electrocautery device, and to prevent secondary burns from a hot tip.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K232407 · printed Nov 5, 2026

Cite this page

510(k) Report. “K232407: Cautery Protective Actuation System (CPAS).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K232407

Report an extraction error

Are you the manufacturer?

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