Wilde-USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wilde-USA, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Wilde-USA, Inc. has 16 FDA 510(k) cleared dental devices. Based in Naperville, US.
Historical record: 16 cleared submissions from 1991 to 1993.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wilde-USA, Inc.
16 devices
Cleared
Jun 24, 1993
COMPATIT R
Dental
682d
Cleared
Apr 08, 1993
KERAMAIL
Dental
477d
Cleared
Feb 26, 1993
WILDE ADHESIVE BONDING SYSTEM
Dental
564d
Cleared
Oct 13, 1992
COMPACOLOR
Dental
91d
Cleared
Jul 23, 1992
COMPASEP
General Hospital
162d
Cleared
Apr 21, 1992
WILDE LIGHT CURING COMPOSITE RESTORATIVE RESINS
Dental
284d
Cleared
Apr 21, 1992
WIL-PDS & WIL-PDI CASTING ALLOYS
Dental
158d
Cleared
Mar 25, 1992
CONVERBASE
Dental
261d
Cleared
Mar 20, 1992
WIL-O-DONT ORTHODONTIC MATERIAL/WIL-O-LUX
Dental
44d
Cleared
Mar 02, 1992
KERALLOY-D CAPS
Dental
75d
Cleared
Feb 03, 1992
WILDE DENTURE RESINS
Dental
210d
Cleared
Dec 23, 1991
COMPALUX STROBOSCOPIC LIGHT POLYMERIZATION DEVICE
Dental
168d
Cleared
Dec 19, 1991
WILDE AUXILIARIES
Dental
164d
Cleared
Nov 13, 1991
KERALLOY NON-GAMMA 2 AMALGAM
Dental
128d
Cleared
Nov 13, 1991
CONVERSIL FL AND CONVERSIL P
Dental
93d
Cleared
Aug 16, 1991
PLANUSTAR AND DENS NOBILIS DENTURE TEETH
Dental
39d