Medical Device Manufacturer · US , Naperville , IL

Wilde-USA, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1991

16

Total

16

Cleared

0

Denied

FDA 510(k) Regulatory Record - Wilde-USA, Inc. Dental ✕

15 devices

1-15 of 15

Cleared Jun 24, 1993

Cleared Apr 08, 1993

Cleared Feb 26, 1993

WILDE ADHESIVE BONDING SYSTEM

Cleared Oct 13, 1992

Cleared Apr 21, 1992

WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS

Cleared Apr 21, 1992

WIL-PDS & WIL-PDI CASTING ALLOYS

Cleared Mar 25, 1992

Cleared Mar 20, 1992

WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX

Cleared Mar 02, 1992

KERALLOY-D CAPS

Cleared Feb 03, 1992

WILDE DENTURE RESINS

Cleared Dec 23, 1991

COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICE

Cleared Dec 19, 1991

WILDE AUXILIARIES

Cleared Nov 13, 1991

KERALLOY NON-GAMMA 2 AMALGAM

Cleared Nov 13, 1991

CONVERSIL FL AND CONVERSIL P

Cleared Aug 16, 1991

PLANUSTAR AND DENS NOBILIS DENTURE TEETH