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Jeneric Ind.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
25
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K862822REXILLIUM N. B. F.September 2, 1986
K862926SURGICAL VITEXAugust 29, 1986
K854878H40 BASE METAL ALLOYJanuary 30, 1986
K844123RX CBYJanuary 9, 1985
K844122RX CBGJanuary 9, 1985
K840563RX C & B 20May 1, 1984
K840561RX ELANMay 1, 1984
K840562REX VApril 13, 1984
K834560VITEX P.D.AFebruary 27, 1984
K833774NATURELLE II & LITE II-N72-N74-LJanuary 24, 1984
K833736GOLD-PALLADIUM-SILVER BASED CAST/ALLOYDecember 29, 1983
K833143REXILLIUM IIIDecember 8, 1983
K833145ZENITHNovember 28, 1983
K833053Y CERAMICNovember 14, 1983
K833052RXGNovember 14, 1983
K833050RX 90October 28, 1983
K833144REX ALLOYOctober 28, 1983
K833049PALLADENTOctober 28, 1983
K823008NOVAREXNovember 3, 1982
K822947NEPTUNEOctober 26, 1982