510(k) · Cleared

Cleared

Anchor Tissue Retrieval System by CONMED

K173822510(k) TraditionalCleared Sep 11, 2018267-day reviewClass II21 CFR 876.1500

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

Conmed Corporation · GCJ Laparoscope, General & Plastic Surgery

Cleared on Sep 11, 2018 as substantially equivalent to K172940 (Conmed Corporation, 2017) after a 267-day review. Its family tree reaches back 2 generations to 2009.

Decided: Sep 11, 2018
Review: 267 days
Class: Class II
Product code: GCJ
Recalls: None
Predicates: 1

Its longest line of descent runs back 2 generations to K091930 (2009). No later device cites it as a predicate yet.

By dateBy generation

Root · 2 generations backK091930 Anchor Laparoscopic Tissue Retrieval System, Model TRS100SBAnchor Products Co. · 2009
1 generation backK172940 ANCHOR Tissue Retrieval SystemConmed Corporation · 2017 · Recalled
This deviceK173822 Anchor Tissue Retrieval System by CONMEDConmed Corporation · 2018

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K091930	Anchor Laparoscopic Tissue Retrieval System, Model TRS100SB	Anchor Products Co.	2009	—
−1	K172940	ANCHOR Tissue Retrieval System	Conmed Corporation	2017	6
0 (this device)	K173822	Anchor Tissue Retrieval System by CONMED	Conmed Corporation	2018	—

FIG. 1 — Lineage of K173822, 2009–2018Source: 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 GCJ? 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 GCJ device

#1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 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? (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
*	K172940	ANCHOR Tissue Retrieval System Summary page 4 …e Primary Device Name: Anchor Tissue Retrieval System Company Name: CONMED Corporation 510(k): K172940 This predicate has not been the subject to a design-related recall. E. Device Description The Anchor™ Tissue Re…	Conmed Corporation	2017	6

Also cleared against K172940: 1 other device →

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 9 years and passes through 2 companies; a new generation was cleared every 8.1 years on median.
1 of the 2 ancestors has a recall of any class.
1 other device also cites its predicate K172940.

How does its category compare?

All GCJ devices

GCJ Laparoscope, General & Plastic Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · GCJ

21in 2025

2007high 31 (2023) · low 15 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GCJ

108in 2025

2007high 122 (2010) · low 42 (2007)2026

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

Recalls per year · GCJ

5in 2025

2007high 30 (2010) · low 0 (2015)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · GCJ

5,860in 2025

2007high 6,047 (2024) · low 1,319 (2008)2025

MAUDE reports naming product code GCJ, 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	18	42	12	1,639
2008	19	73	16	1,319
2009	21	85	6	1,995
2010	24	122	30	2,657
2011	15	113	9	2,133
2012	17	88	1	1,526
2013	15	93	7 (1)	1,565
2014	19	90	2	1,714
2015	26	76	0	1,710
2016	27	99	5	2,080
2017	20	77	1	3,468
2018	21	88	1	2,562
2019	15	60	0	2,578
2020	28	61	0	2,618
2021	18	116	0	3,431
2022	20	103	1	3,945
2023	31	109	1	6,002
2024	29	90	0	6,047
2025	21	108	5	5,860
2026	26	122	1	—

What is it indicated for?

The Anchor™ Tissue Retrieval System™ by CONMED is a sterile disposable pouch used with a dedicated introducer for the encapture and transvaginal removal of an organ or tissue during laparoscopic hysterectomy.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K173822 · printed Nov 6, 2026

Cite this page

510(k) Report. “K173822: Anchor Tissue Retrieval System by CONMED.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K173822

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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