510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K904349Substantially Equivalent

Cui Curvilinear Silicone Chin

Cui Corp., Santa Barbara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K904349 is the FDA 510(k) clearance record for CUI CURVILINEAR SILICONE CHIN, a class II device, cleared for Cui Corp. on under FDA product code FWP (Prosthesis, Chin, Internal). FDA records list 7 510(k) clearances for Cui Corp., from to . As of , FDA records show no recalls naming K904349.

Clearance record

Decision date
Received
(63 days to decision)
Product code
FWP Prosthesis, Chin, Internal
Regulation
21 CFR 878.3550
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Cui Corp. P.O. Box 40288, Santa Barbara CA
Third party review
No

Clearances, product code FWP

Trailing 12 months
1 clearance under product code FWP in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FWP, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260