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VCARE
Model 60-6085-200A · Conmed Corporation · DI 10653405003748
LKF — Cannula, Manipulator/Injector, Uterine · Class II · 21 CFR 884.4530
UDILibrary device dossier · generated 2026-09-15 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.
Recall history (0)
No recalls linked in the loaded window.
Adverse-event reports — MAUDE (106)
Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.
Malfunction: 98 · Injury: 7 · Other: 1
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
0
2
2019-02
0
1.8
2019-03
0
4.33
2019-04
1
4.33
2019-05
2
4.67
2019-06
5
3.5
2019-07
2
2
2019-08
2
3.67
2019-09
0
2
2019-10
3
3.5
2019-11
1
1
2019-12
0
1.67
2020-01
0
2.4
2020-02
3
2
2020-03
2
3.8
2020-04
2
2.83
2020-05
0
1
2020-06
4
4.5
2020-07
1
4
2020-08
1
1.71
2020-09
0
3.75
2020-10
0
4
2020-11
0
7
2020-12
1
2.17
2021-01
1
2.2
2021-02
2
4
2021-03
7
4.5
2021-04
3
3.6
2021-05
2
3.17
2021-06
4
6
2021-07
0
13
2021-08
3
4.25
2021-09
1
6
2021-10
0
1.67
2021-11
5
3.5
2021-12
3
7.5
2022-01
0
1
2022-02
0
2.5
2022-03
0
4.25
2022-04
0
2.75
2022-05
0
2.67
2022-06
1
2.5
2022-07
0
4.33
2022-08
0
2.25
2022-09
0
2
2022-10
1
2.5
2022-11
0
2.67
2022-12
0
2
2023-01
0
6.5
2023-02
1
1.8
2023-03
2
2
2023-04
1
1.5
2023-05
0
7.5
2023-06
1
1.75
2023-07
2
2
2023-08
1
1.8
2023-09
1
1.33
2023-10
0
2
2023-11
2
2.33
2023-12
0
2
2024-01
2
4
2024-02
1
2.83
2024-03
0
1.67
2024-04
4
3.33
2024-05
2
1.67
2024-06
0
1
2024-07
2
2.75
2024-08
2
4.33
2024-09
0
8
2024-10
0
3
2024-11
0
3.33
2024-12
1
3
2025-01
3
4.33
2025-02
0
3.67
2025-03
0
1.5
2025-04
1
3
2025-05
2
3
2025-06
1
2.67
2025-07
0
3
2025-08
0
1
2025-09
0
2
2025-10
4
2.67
2025-11
1
3.67
2025-12
2
2.25
2026-01
0
3.67
2026-02
0
3
2026-03
0
3.5
2026-04
3
2.5
2026-05
0
16
2026-06
1
3.33
This device (reports/month)Average device in LKF (reports/device/month)
Regulatory clearances
K142716 SESE 2015-02-10 (k number procode)
Predicate lineage
K142716 — cites (transitively): K071907 (d1) — cited as predicate by K220202
Lineage extracted from public 510(k) summary text (heuristic).
Manufacturer compliance record — Conmed Corporation