Cui Corp.
Medical device manufacturer in Santa Barbara, CA.
7510(k) clearances
0PMA approvals
0recalls
Device types
510(k) clearances
| 510(k) | Device | Decision |
|---|---|---|
| K913140 | Silicone Gel SheetingMDA · Traditional | 09/30/1991SE |
| K904350 | Cui Dorsal Columella ProsthesisFZE · Traditional | 11/26/1990SE |
| K904349 | Cui Curvilinear Silicone ChinFWP · Traditional | 11/26/1990SE |
| K904348 | Cui Feathered Silicone MalarLZK · Traditional | 11/26/1990SE |
| K903329 | Cui Anatomical Silicone MalarLZK · Traditional | 09/10/1990SE |
| K903328 | Cui Premaxillary ImplantFZE · Traditional | 09/10/1990SE |
| K903327 | Cui Articulated Silicone ChinFWP · Traditional | 09/10/1990SE |