510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K831566Substantially Equivalent

Cui Mammary Prothesis Sizer

Cox-Uphuff Intl., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K831566 is the FDA 510(k) clearance record for CUI MAMMARY PROTHESIS SIZER, cleared for Cox-Uphuff Intl. on under FDA product code MRD (Mammary Sizer). FDA records list 11 510(k) clearances for Cox-Uphuff Intl., from to . As of , FDA records show 2 recalls naming K831566.

Clearance record

Decision date
Received
(88 days to decision)
Product code
MRD Mammary Sizer
Device class
Unclassified
Review panel
Unknown
Applicant
Cox-Uphuff Intl. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code MRD

Trailing 12 months

FDA records hold no clearances under product code MRD in the trailing twelve months.

FDA records show no clearances under product code MRD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code MRD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260