Ultimate Wireforms, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K960799ORTHO-ICEMay 9, 1996
K923837DIMPLED MULTI MODULUS ARCH WIREMarch 31, 1993
K924805ORTHODONTIC ARCH WIREMarch 31, 1993
K923836.016' X .016 NICKEL TITANIUM UPRIGHTING SPRINGDecember 23, 1992
K923838THE ULTIMATE RCS ARCH WIREDecember 4, 1992
K923839NITINOL GENTLE TOUCH COIL SPRINGOctober 15, 1992