Cui Corp.

Cui Corp. holds 7 FDA 510(k) medical device clearances, first cleared 1990, most recent 1991.

Top product codes for Cui Corp.

Recent clearances by Cui Corp.

K913140 — SILICONE GEL SHEETINGCode MDA·1991-09-30
K904348 — CUI FEATHERED SILICONE MALARCode LZK·1990-11-26
K904349 — CUI CURVILINEAR SILICONE CHINCode FWP·1990-11-26
K904350 — CUI DORSAL COLUMELLA PROSTHESISCode FZE·1990-11-26
K903327 — CUI ARTICULATED SILICONE CHINCode FWP·1990-09-10
K903328 — CUI PREMAXILLARY IMPLANTCode FZE·1990-09-10
K903329 — CUI ANATOMICAL SILICONE MALARCode LZK·1990-09-10

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