Medical Device Manufacturer · US , Terryville , CT

Ultimate Wireforms, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ultimate Wireforms, Inc. Dental ✕

6 devices

1-6 of 6

Cleared May 09, 1996

Cleared Mar 31, 1993

DIMPLED MULTI MODULUS ARCH WIRE

Cleared Mar 31, 1993

ORTHODONTIC ARCH WIRE

Cleared Dec 23, 1992

.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING

Cleared Dec 04, 1992

THE ULTIMATE RCS ARCH WIRE

Cleared Oct 15, 1992

NITINOL GENTLE TOUCH COIL SPRING

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026