Cui Corp.

7 FDA 510(k) medical device clearances.

Top product codes for Cui Corp.

FWP — General, Plastic Surgery 2 devices
FZE — General, Plastic Surgery 2 devices
LZK — General, Plastic Surgery 2 devices
MDA — General, Plastic Surgery 1 device

Recent clearances by Cui Corp.

K913140 — SILICONE GEL SHEETING MDA · 1991-09-30
K904348 — CUI FEATHERED SILICONE MALAR LZK · 1990-11-26
K904349 — CUI CURVILINEAR SILICONE CHIN FWP · 1990-11-26
K904350 — CUI DORSAL COLUMELLA PROSTHESIS FZE · 1990-11-26
K903327 — CUI ARTICULATED SILICONE CHIN FWP · 1990-09-10
K903328 — CUI PREMAXILLARY IMPLANT FZE · 1990-09-10
K903329 — CUI ANATOMICAL SILICONE MALAR LZK · 1990-09-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.