510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K871200Substantially Equivalent

Cui Nasal Septum Button

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

K871200 is the FDA 510(k) clearance record for CUI NASAL SEPTUM BUTTON, cleared for Cox-Uphuff Intl. on under FDA product code LFB (Button, Nasal Septal). FDA records list 11 510(k) clearances for Cox-Uphuff Intl., from to . As of , FDA records show no recalls naming K871200.

Clearance record

Decision date
Received
(21 days to decision)
Product code
LFB Button, Nasal Septal
Device class
Unclassified
Review panel
Unknown
Applicant
Cox-Uphuff Intl. 1160 Mark Ave., Carpinteria CA
Third party review
No

Clearances, product code LFB

Trailing 12 months

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

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