Not currently registered with FDA under this name

Wilde-USA, Inc.

Chicago, IL, United States. Named as applicant on 15 dental 510(k) clearances between 1991 and 1993. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 151991–1993
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1990–2026

510(k) clearances

Clearances on which FDA names Wilde-USA, Inc. as the applicant.

Decided	510(k)	Device	Device type
24 Jun 1993	K913582	COMPATIT R	ELM Teeth Plastic Denture
8 Apr 1993	K915653	KERAMAIL	EIH Porcelain Powder
26 Feb 1993	K913581	WILDE ADHESIVE BONDING SYSTEM	KLE Resin Tooth Bonding Agent
13 Oct 1992	K923472	COMPACOLOR	EBF Resin Tooth Shade Material
21 Apr 1992	K915250	WIL-PDS & WIL-PDI CASTING ALLOYS	EJH Base Metal Alloy
21 Apr 1992	K913089	WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS	EBF Resin Tooth Shade Material
25 Mar 1992	K912990	CONVERBASE	EBI Rebasing Repairing Relining Denture Resin
20 Mar 1992	K920557	WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX	EBI Rebasing Repairing Relining Denture Resin
2 Mar 1992	K915654	KERALLOY-D CAPS	EJJ Amalgam Alloy
3 Feb 1992	K912993	WILDE DENTURE RESINS	EBI Rebasing Repairing Relining Denture Resin
23 Dec 1991	K912994	COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICE	EBZ Ultraviolet Activator for Polymerization
19 Dec 1991	K912991	WILDE AUXILIARIES	EBI Rebasing Repairing Relining Denture Resin
13 Nov 1991	K913583	CONVERSIL FL AND CONVERSIL P	ELW Impression Material
13 Nov 1991	K912992	KERALLOY NON-GAMMA 2 AMALGAM	EJJ Amalgam Alloy
16 Aug 1991	K912989	PLANUSTAR AND DENS NOBILIS DENTURE TEETH	EMI Surgical Bone File

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.