510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MRDUnclassified

Mammary Sizer

Unknown
FDA source (opens on fda.gov)

MRD is the FDA product code for Mammary Sizer. As of , FDA records hold 13 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
MRD
Device name
Mammary Sizer
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
13
Ingested recalls
4

Clearances, product code MRD

By decision year
13 clearances under product code MRD with a decision year between 1983 and 2025, 1983 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MRD by decision year
YearClearances
19831
19961
19981
19991
20011
20061
20131
20151
20191
20201
20211
20241
20251

Applicants with the most clearances

Product code MRD
Applicants holding the most 510(k) clearances under product code MRD
ApplicantClearances
Mentor Worldwide, LLC4
Mentor2
Specialty Surgical Products, Inc.2
Allergan1
Cox-Uphuff Intl.1
General Surgical Innovations1
Motiva USA, LLC1
Sientra, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code