Spinalight, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
4
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K172536Atlas Percussion Adjusting InstrumentJune 20, 2018
K001476TORQUE INSTRUMENT, MODEL 8500August 4, 2000
K955540HAND HELD ATLAS INSTRUMENTMarch 4, 1996
K946258MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENTNovember 20, 1995
K945954MODELS 4100 AND 4300 MULTITHERAPYJanuary 19, 1995
K933622FLEXION DISTRACTION TABLEJanuary 7, 1994
K933621HILO TABLEJanuary 7, 1994