510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K853945Substantially Equivalent

Cui Rhinoplasty Implants

Cox-Uphuff Intl., Santa Barbara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853945 is the FDA 510(k) clearance record for CUI RHINOPLASTY IMPLANTS, a class II device, cleared for Cox-Uphuff Intl. on under FDA product code FZE (Prosthesis, Nose, Internal). FDA records list 11 510(k) clearances for Cox-Uphuff Intl., from to . As of , FDA records show no recalls naming K853945.

Clearance record

Decision date
Received
(24 days to decision)
Product code
FZE Prosthesis, Nose, Internal
Regulation
21 CFR 878.3680
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cox-Uphuff Intl. 725 E. Yanonali St., Santa Barbara CA
Third party review
No

Clearances, product code FZE

Trailing 12 months

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

FDA records show no clearances under product code FZE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FZE, 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