Medical Device Manufacturer · US , Santa Barbara , CA

Cui Corp. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1990

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Cui Corp. General & Plastic Surgery ✕

7 devices

1-7 of 7

Cleared Sep 30, 1991

SILICONE GEL SHEETING

General & Plastic Surgery · 76d

Cleared Nov 26, 1990

CUI FEATHERED SILICONE MALAR

General & Plastic Surgery · 63d

Cleared Nov 26, 1990

CUI CURVILINEAR SILICONE CHIN

General & Plastic Surgery · 63d

Cleared Nov 26, 1990

CUI DORSAL COLUMELLA PROSTHESIS

General & Plastic Surgery · 63d

Cleared Sep 10, 1990

CUI ARTICULATED SILICONE CHIN

General & Plastic Surgery · 47d

Cleared Sep 10, 1990

CUI PREMAXILLARY IMPLANT

General & Plastic Surgery · 47d

Cleared Sep 10, 1990

CUI ANATOMICAL SILICONE MALAR

General & Plastic Surgery · 47d