Wilde-USA, Inc.
FDA 510(k) & PMA Approved Devices — 16 products
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Total Devices16
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K913582 | COMPATIT R | ELM | 1993-06-24 | View |
| 510(k) | K915653 | KERAMAIL | EIH | 1993-04-08 | View |
| 510(k) | K913581 | WILDE ADHESIVE BONDING SYSTEM | KLE | 1993-02-26 | View |
| 510(k) | K923472 | COMPACOLOR | EBF | 1992-10-13 | View |
| 510(k) | K920649 | COMPASEP | FMC | 1992-07-23 | View |
| 510(k) | K915250 | WIL-PDS & WIL-PDI CASTING ALLOYS | EJH | 1992-04-21 | View |
| 510(k) | K913089 | WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS | EBF | 1992-04-21 | View |
| 510(k) | K912990 | CONVERBASE | EBI | 1992-03-25 | View |
| 510(k) | K920557 | WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX | EBI | 1992-03-20 | View |
| 510(k) | K915654 | KERALLOY-D CAPS | EJJ | 1992-03-02 | View |
| 510(k) | K912993 | WILDE DENTURE RESINS | EBI | 1992-02-03 | View |
| 510(k) | K912994 | COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICE | EBZ | 1991-12-23 | View |
| 510(k) | K912991 | WILDE AUXILIARIES | EBI | 1991-12-19 | View |
| 510(k) | K913583 | CONVERSIL FL AND CONVERSIL P | ELW | 1991-11-13 | View |
| 510(k) | K912992 | KERALLOY NON-GAMMA 2 AMALGAM | EJJ | 1991-11-13 | View |
| 510(k) | K912989 | PLANUSTAR AND DENS NOBILIS DENTURE TEETH | EMI | 1991-08-16 | View |
No matching devices.
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