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L11
Model 0220230300 · STRYKER CORPORATION · DI 07613327455915
OWN — Confocal Optical Imaging · Class II · 21 CFR 876.1500
UDILibrary device dossier · generated 2026-09-06 · 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 (236)
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: 228 · Injury: 8
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
1
2019-03
0
1
2019-04
0
2
2019-05
0
2
2019-06
0
1.67
2019-07
1
1.5
2019-08
1
1.5
2019-09
1
1
2019-10
1
2.75
2019-11
4
2.5
2019-12
5
5
2020-01
2
1.67
2020-02
0
2.5
2020-03
3
1.67
2020-04
1
1
2020-05
0
1.5
2020-06
5
4
2020-07
1
2.17
2020-08
4
2.2
2020-09
4
2.6
2020-10
2
3.33
2020-11
1
2
2020-12
1
2.33
2021-01
3
3.4
2021-02
2
2
2021-03
1
3.43
2021-04
1
5.4
2021-05
1
2.88
2021-06
1
2.88
2021-07
1
3.29
2021-08
0
3.38
2021-09
0
4.25
2021-10
2
3
2021-11
2
3.29
2021-12
3
6
2022-01
2
3.71
2022-02
0
8.4
2022-03
2
6.33
2022-04
4
5.83
2022-05
5
12.63
2022-06
7
10.83
2022-07
2
5.57
2022-08
1
4.4
2022-09
2
3.9
2022-10
4
4.38
2022-11
0
5.9
2022-12
5
4.75
2023-01
2
5.29
2023-02
6
4.63
2023-03
7
6.27
2023-04
8
7.25
2023-05
7
7.75
2023-06
2
4.7
2023-07
4
6.75
2023-08
3
8
2023-09
6
10.14
2023-10
4
7.44
2023-11
7
8.22
2023-12
3
8.88
2024-01
4
7.91
2024-02
5
15.86
2024-03
2
14
2024-04
4
11.11
2024-05
4
11.71
2024-06
1
18.83
2024-07
1
22.4
2024-08
6
13
2024-09
1
12.86
2024-10
1
13.71
2024-11
2
6.25
2024-12
12
9.67
2025-01
5
8
2025-02
2
3.63
2025-03
1
5.5
2025-04
3
4.33
2025-05
2
4.4
2025-06
3
5
2025-07
4
6.88
2025-08
4
4.8
2025-09
0
3.83
2025-10
5
4.23
2025-11
1
3.71
2025-12
3
4.79
2026-01
0
4.9
2026-02
2
3.5
2026-03
5
4
2026-04
2
6.21
2026-05
1
4.2
2026-06
3
3.87
This device (reports/month)Average device in OWN (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