• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Mainstay Medical Limited ReActiv8; ReActiv8 Implantable Pulse Generator

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

Mainstay Medical Limited ReActiv8; ReActiv8 Implantable Pulse Generator Back to Search Results
Model Number 5100
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Implant Pain (4561)
Date of Event 08/14/2026
Type of Reportable Event Serious Injury
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
ReActiv8
Common Device Name
ReActiv8 Implantable Pulse Generator
Manufacturer (Section D)
Mainstay Medical Limited
clonmel house, forster way
swords, co. dublin K67F2 K3
EI  K67F2K3
Manufacturer Contact
liza dominguez
2159 india street
suite 200
san diego, CA 92101
+1(619)206-3331
MDR Report Key50744597
Report Number3021520203-2026-00110
Device Sequence Number8494597
Product Code QLK
UDI-Device Identifier05391527770015
UDI-Public0105391527770015112506171727071421715210H5537
Combination Product (Y/N)N
Initial Reporter CountryGM
PMA/510(K) Number
P190021
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2026
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Company Representative
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 09/11/2026
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 Number5100
Device Catalogue Number5100
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 08/14/2026
Initial Report FDA Received Date09/11/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured06/17/2025
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 Age49 YR
Patient SexMale
Patient Weight154 LB
-
-