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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Axonics Modulation Technologies, Inc. Axonics; Stimulator, Electrical, Implantable, For Incontinence

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Axonics Modulation Technologies, Inc. Axonics; Stimulator, Electrical, Implantable, For Incontinence Back to Search Results
Model Number 1701
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Unspecified Tissue Injury (4559)
Date of Event 07/15/2024
Type of Reportable Event Serious Injury
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Brand Name
Axonics
Common Device Name
Stimulator, Electrical, Implantable, For Incontinence
Manufacturer (Section D)
Axonics Modulation Technologies, Inc.
15515 sand canyon ave
irvine CA 92618
Manufacturer (Section G)
Axonics Inc
15515 sand canyon ave
irvine CA 92618
Manufacturer Contact
farshad fahimi
4100 hamline avenue north
building c
saint paul, MN 55112
MDR Report Key50941036
Report Number2124215-2026-51865
Device Sequence Number13442381
Product Code EZW
UDI-Device Identifier10810005340134
UDI-Public(01)10810005340134
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
P180046
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Remedial Action Recall
Type of Report Initial
Report Date (Section B) 09/29/2026
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Operator of Device Health Professional
Device Model Number1701
Device Catalogue Number1701
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 07/15/2024
Initial Report FDA Received Date09/29/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Initial
Patient Sequence Number1
Outcome Attributed to Adverse Event Other;
Patient SexUnknown
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