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Dyonics, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
19
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K900070MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEMFebruary 16, 1990
K896416DYONICS SHOULDER PORTAL SYSTEMJanuary 2, 1990
K893136SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTYDecember 14, 1989
K890665MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIESNovember 3, 1989
K894728DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFEAugust 18, 1989
K892062PS3500 ARTHROSCOPIC SURGICAL SYSTEMJune 23, 1989
K884839MODIFIED SAW BLADES TO THE SAGITAL SAWDecember 7, 1988
K881876DYNAMIC CRUCIATE TESTERNovember 17, 1988
K880739DYONICS DRILL GUIDE/ISOMETER SYSTEMMarch 21, 1988
K880150PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEMMarch 4, 1988
K870212ARTHROSCOPIC SHOULDER HOLDERFebruary 20, 1987
K862017ARTHROSCOPIC SHOULDER LIGAMENT REPAIR KITDecember 15, 1986
K843121GUIDE TO THE KNEESeptember 7, 1984
K833943MENISCAL SUTURING SYSTEMFebruary 27, 1984
K833587DISPOSABLE ARTHROSCOPY BLADENovember 14, 1983
K820367INTRA-ARTICULAR SURGICAL SYSTEMMay 7, 1982
K812506THE ARTHROFILESeptember 24, 1981
K790502DYONICS STEROTOXIC POSITIONERApril 5, 1979
K771218INTRA-ARTICULAR SHAVERFebruary 1, 1978