Cui Corp.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K913140 | SILICONE GEL SHEETING | MDA | 1991-09-30 | View |
| 510(k) | K904349 | CUI CURVILINEAR SILICONE CHIN | FWP | 1990-11-26 | View |
| 510(k) | K904350 | CUI DORSAL COLUMELLA PROSTHESIS | FZE | 1990-11-26 | View |
| 510(k) | K904348 | CUI FEATHERED SILICONE MALAR | LZK | 1990-11-26 | View |
| 510(k) | K903329 | CUI ANATOMICAL SILICONE MALAR | LZK | 1990-09-10 | View |
| 510(k) | K903328 | CUI PREMAXILLARY IMPLANT | FZE | 1990-09-10 | View |
| 510(k) | K903327 | CUI ARTICULATED SILICONE CHIN | FWP | 1990-09-10 | View |
No matching devices.
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