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Ruggles Corp.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K903485
TITANIUM MESH
February 21, 1991
K902818
MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT
September 20, 1990
K902819
LAMINECTOMY ROGEUR
August 9, 1990
K902850
ZEPPELIN INSTRUMENTS
July 18, 1990
K893415
TRANS-ORAL DEPTH GAUGE
June 7, 1989