Ultimate Wireforms, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ultimate Wireforms, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Ultimate Wireforms, Inc. has 6 FDA 510(k) cleared medical devices. Based in Terryville, US.
Historical record: 6 cleared submissions from 1992 to 1996. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ultimate Wireforms, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ultimate Wireforms, Inc.
6 devices
Cleared
May 09, 1996
ORTHO-ICE
Dental
72d
Cleared
Mar 31, 1993
DIMPLED MULTI MODULUS ARCH WIRE
Dental
244d
Cleared
Mar 31, 1993
ORTHODONTIC ARCH WIRE
Dental
188d
Cleared
Dec 23, 1992
.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING
Dental
146d
Cleared
Dec 04, 1992
THE ULTIMATE RCS ARCH WIRE
Dental
127d
Cleared
Oct 15, 1992
NITINOL GENTLE TOUCH COIL SPRING
Dental
77d