510(k) Report

510(k) · Cleared

Recalled · 2006

Conmed Selectone Minimal Access Surgery Instruments

K943327510(k) TraditionalCleared Nov 7, 1994118-day reviewClass II21 CFR 876.1500Recalls 22

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

Conmedcorp · GCJ Laparoscope, General & Plastic Surgery

Cleared on Nov 7, 1994 after a 118-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. It has been recalled 22 times.

Decided
Nov 7, 1994
Review
118 days
Class
Class II
Product code
GCJ
Recalls
22
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K943327Source: FDA 510(k) database · 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), 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. #1 K214046 780 nm 1688 4K Camera System, 780 nm L11 LED…score 21.4 · 21 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Oct 12, 2006Not classifiedZ-0094-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0096-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0101-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0103-2007Nonconforming Material/ComponentThe company was made aware of instances where the grasper jaws broke during laparoscopic procedures. When the grasper jaws had broken they had done so at the junction of the jaw and the tube. In no instances was it reported to the company…
Oct 12, 2006Not classifiedZ-0112-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0113-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0114-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0093-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0108-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0109-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0097-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0100-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0102-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0105-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0106-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0107-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0095-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0098-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0099-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0104-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0110-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.
Oct 12, 2006Not classifiedZ-0111-2007Nonconforming Material/ComponentThe grasper jaws broke during laparoscopic procedures at the junction of the jaw and the tube.

The 5 latest of 22 recalls; the web page lists all.

No ancestor or descendant has a Class I recall.

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.

FDA decisions per year · GCJ

21in 2025

2007: 182008: 192009: 212010: 242011: 152012: 172013: 152014: 192015: 262016: 272017: 202018: 212019: 152020: 282021: 182022: 202023: 312024: 292025: 212026 (partial year): 26
2007high 31 (2023) · low 15 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GCJ

108in 2025

2007: 42 days median2008: 73 days median2009: 85 days median2010: 122 days median2011: 113 days median2012: 88 days median2013: 93 days median2014: 90 days median2015: 76 days median2016: 99 days median2017: 77 days median2018: 88 days median2019: 60 days median2020: 61 days median2021: 116 days median2022: 103 days median2023: 109 days median2024: 90 days median2025: 108 days median2026 (partial year): 122 days median
2007high 122 (2010) · low 42 (2007)2026

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

Recalls per year · GCJ

5in 2025

2007: 122008: 162009: 62010: 302011: 92012: 12013: 7, 1 Class I2014: 22016: 52017: 12018: 12022: 12023: 12025: 52026 (partial year): 1
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

2007: 1,6392008: 1,3192009: 1,9952010: 2,6572011: 2,1332012: 1,5262013: 1,5652014: 1,7142015: 1,7102016: 2,0802017: 3,4682018: 2,5622019: 2,5782020: 2,6182021: 3,4312022: 3,9452023: 6,0022024: 6,0472025: 5,860
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071842121,639
20081973161,319
2009218561,995
201024122302,657
20111511392,133
2012178811,526
201315937 (1)1,565
2014199021,714
2015267601,710
2016279952,080
2017207713,468
2018218812,562
2019156002,578
2020286102,618
20211811603,431
20222010313,945
20233110916,002
2024299006,047
20252110855,860
2026261221—

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https://510kreport.com/device/K943327 · printed Nov 6, 2026

Cite this page

510(k) Report. “K943327: Conmed Selectone Minimal Access Surgery Instruments.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K943327

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026