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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Mentor Texas MENTOR MemoryGel BOOST Breast Implant; Prosthesis, breast, noninflatable, internal, silicone gel-filled

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Mentor Texas MENTOR MemoryGel BOOST Breast Implant; Prosthesis, breast, noninflatable, internal, silicone gel-filled Back to Search Results
Catalog Number SMPB480
Medical Device Problem Code Migration (4003)
Health Effect - Clinical Code Deformity/ Disfigurement (2360)
Date of Event 07/28/2025
Type of Reportable Event Serious Injury
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Brand Name
MENTOR MemoryGel BOOST Breast Implant
Common Device Name
Prosthesis, breast, noninflatable, internal, silicone gel-filled
Manufacturer (Section D)
Mentor Texas
3041 skyway circle north
irving TX 75038
Manufacturer (Section G)
Mentor Texas
3041 skyway circle north
irving TX 75038
Manufacturer Contact
henry boden
3041 skyway circle north
irving, TX 75038
+1(949)788-2078
MDR Report Key50933898
Report Number1645337-2026-10800
Device Sequence Number9689026
Product Code FTR
UDI-Device Identifier00081317026914
Combination Product (Y/N)N
Initial Reporter StateOK
Initial Reporter CountryUS
PMA/510(K) Number
P030053
Number of Events Summarized1
Summary Report (Y/N)N
Device Implanted Year2025
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional
Type of Report Initial
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? Yes
Operator of Device Health Professional
Device Catalogue NumberSMPB480
Device Lot Number2021857
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Received by Manufacturer 09/17/2026
Initial Report FDA Received Date09/29/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured12/10/2024
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 Age59 YR
Patient SexFemale
Patient RaceWhite
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