Product code MRD— Unknown

FDA has cleared 13 devices under product code MRD between 1983 and 2025, filed by 9 applicant companies. No FDA device recalls reference this product code.

• 20251 clearance
• 20241 clearance
• 20211 clearance
• 20201 clearance
• 20191 clearance
• 20151 clearance
• 20131 clearance
• 20061 clearance
• 20011 clearance
• 19991 clearance
• 19981 clearance
• 19961 clearance
• 19831 clearance

• Mentor Worldwide, LLC4 clearances
• Specialty Surgical Products, Inc.2 clearances
• Sientra, Inc.1 clearance
• Motiva USA, LLC1 clearance
• Mentor Corporation1 clearance
• Mentor Corp.1 clearance
• General Surgical Innovations1 clearance
• Cox-Uphuff Intl.1 clearance
• Allergan1 clearance

• K243271 — MENTOR MemoryShape Resterilizable Gel Breast Implant Sizer +2 moreMentor Worldwide, LLC·2025-01-13
• K241552 — MENTOR MemoryGel Enhance Single Use Gel SizerMentor Worldwide, LLC·2024-09-06
• K203229 — NATRELLE INSPIRA Single Use Sizers for Gel ImplantsAllergan·2021-06-02
• K200706 — Sientra OPUS Silicone Gel Breast Implant SizerSientra, Inc.·2020-11-16
• K183163 — Intraoperative, Single-Use, Sterile, Silicone Breast Sizer Motiva Implant MatrixMotiva USA, LLC·2019-02-05
• K151055 — Mentor MemoryShape Resterilizable Gel Breast Implant Sizer STERILEMentor Worldwide, LLC·2015-05-20
• K131853 — MENTOR MEMORYSHAPE RESTERILIZABLE GEL SIZERMentor Worldwide, LLC·2013-07-17
• K062421 — MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZERMentor Corporation·2006-10-10
• K010709 — MENTOR STERILE SALINE MAMMARY VOLUME SIZERSMentor Corp.·2001-04-23
• K984106 — MAMMARY SIZER, MAMMARY PROTHESIS SIZERSpecialty Surgical Products, Inc.·1999-02-12
• K982258 — MAMMARY SIZERSpecialty Surgical Products, Inc.·1998-09-08
• K961356 — MAMMARY SIZERGeneral Surgical Innovations·1996-09-23
• K831566 — CUI MAMMARY PROTHESIS SIZERCox-Uphuff Intl.·1983-08-12