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Neptune
Model 0703046000 · STRYKER CORPORATION · DI 07613327117189
GEI — Electrosurgical, Cutting & Coagulation & Accessories · Class II · 21 CFR 878.4400
UDILibrary device dossier · generated 2026-09-13 · 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 (153)
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: 137 · Injury: 16
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
6.86
2019-02
4
4.35
2019-03
1
4.42
2019-04
7
6.12
2019-05
0
4.8
2019-06
0
5.04
2019-07
0
5.86
2019-08
0
6.1
2019-09
0
4.99
2019-10
1
5.85
2019-11
4
5.62
2019-12
15
5.41
2020-01
1
4.81
2020-02
0
5.57
2020-03
7
5.68
2020-04
0
3.57
2020-05
0
3.76
2020-06
0
5.14
2020-07
4
6.56
2020-08
3
4.64
2020-09
0
5.86
2020-10
2
5.55
2020-11
1
5.14
2020-12
0
5.31
2021-01
2
5.17
2021-02
0
4.89
2021-03
0
5.7
2021-04
0
5.26
2021-05
2
5.14
2021-06
4
5.83
2021-07
0
4.89
2021-08
0
4.3
2021-09
1
4.77
2021-10
0
6.17
2021-11
1
5.57
2021-12
0
5.56
2022-01
0
5.04
2022-02
0
5.15
2022-03
0
5.75
2022-04
1
4.98
2022-05
2
5.78
2022-06
1
6.3
2022-07
0
4.36
2022-08
0
4.59
2022-09
1
5
2022-10
1
4.76
2022-11
0
4.61
2022-12
2
4.04
2023-01
2
5.52
2023-02
4
4.59
2023-03
3
4.87
2023-04
1
4.78
2023-05
2
5.14
2023-06
2
4.78
2023-07
2
4.82
2023-08
1
4.44
2023-09
1
5.23
2023-10
1
5.1
2023-11
5
4.38
2023-12
2
4.79
2024-01
1
5.54
2024-02
5
5.46
2024-03
0
6.16
2024-04
4
6.04
2024-05
2
6.28
2024-06
1
5.39
2024-07
2
5.05
2024-08
1
5.01
2024-09
1
5.19
2024-10
3
5.7
2024-11
5
5.29
2024-12
1
4.06
2025-01
2
5.17
2025-02
0
4.46
2025-03
2
6.28
2025-04
2
4.39
2025-05
2
5.16
2025-06
5
5.08
2025-07
0
5.2
2025-08
1
5.45
2025-09
3
4.85
2025-10
2
5.14
2025-11
4
5.55
2025-12
3
5.81
2026-01
2
5.63
2026-02
0
5.98
2026-03
2
6.2
2026-04
0
5.43
2026-05
1
6.19
2026-06
2
5.56
This device (reports/month)Average device in GEI (reports/device/month)
Regulatory clearances
None linked in the loaded window.
Manufacturer compliance record — STRYKER CORPORATION
Warning Letter 2017-04-06 Entellus Medical Inc.
Warning Letter 2015-04-08 Thermedx LLC
Injunction 2013-11-26 Physio-Control, Inc.
Warning Letter 2013-03-06 Stryker Corporation
Warning Letter 2013-03-06 Stryker Corporation
NAI 2026-06-18 International Life Sciences · 0 citations
VAI 2026-02-20 Stryker Puerto Rico, LLC · 2 citations
NAI 2025-12-11 Stryker Manufacturing Kalamazoo · 0 citations
NAI 2025-05-22 Stryker Macroom · 0 citations
VAI 2025-03-27 Stryker GmbH · 1 citations
VAI 2025-03-27 Stryker GmbH · 1 citations
NAI 2025-02-27 Stryker Leibinger GmbH & Co. KG · 0 citations
NAI 2025-01-30 Serf · 0 citations
VAI 2024-12-18 Stryker Neurovascular · 1 citations
VAI 2024-11-15 Stryker Medical Division of Stryker Corporation · 2 citations
NAI 2024-11-13 POM Medical LLC · 0 citations
VAI 2024-07-25 Stryker Ireland, Ltd., Instruments Division · 1 citations
NAI 2024-05-03 Stryker Neurovascular, Inc. · 0 citations
NAI 2024-04-18 Physio-Control, Inc. · 0 citations
VAI 2023-12-01 Howmedica Osteonics Corp. · 1 citations
VAI 2023-05-15 LimFlow, Inc. · 2 citations
NAI 2023-04-25 Stryker Puerto Rico, LLC · 0 citations