Dyonics, Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Dyonics, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Walker, US.
Historical record: 19 cleared submissions from 1978 to 1990.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
19 devices
Cleared
Feb 16, 1990
MODIFIED USES OF THE ARTHROSCOPIC SURGICAL SYSTEM
Orthopedic
43d
Cleared
Jan 02, 1990
DYONICS SHOULDER PORTAL SYSTEM
Orthopedic
55d
Cleared
Dec 14, 1989
SURGI-PAK FOR ARTHROSCOPIC ACROMIOPLASTY
Orthopedic
233d
Cleared
Nov 03, 1989
MODIFIED CANNULA, TROCAR AND OBTURATOR ACCESSORIES
Orthopedic
267d
Cleared
Aug 18, 1989
DYONICS DISPOSABLE ARTHROSCOPIC SURGICAL KNIFE
Orthopedic
23d
Cleared
Jun 23, 1989
PS3500 ARTHROSCOPIC SURGICAL SYSTEM
Orthopedic
85d
Cleared
Dec 07, 1988
MODIFIED SAW BLADES TO THE SAGITAL SAW
Orthopedic
16d
Cleared
Nov 17, 1988
DYNAMIC CRUCIATE TESTER
Neurology
197d
Cleared
Mar 21, 1988
DYONICS DRILL GUIDE/ISOMETER SYSTEM
Orthopedic
26d
Cleared
Mar 04, 1988
PACESETTER (TM) 3500 ARTHROSCOPIC SURGICAL SYSTEM
Orthopedic
51d
Cleared
Feb 20, 1987
ARTHROSCOPIC SHOULDER HOLDER
Neurology
31d
Cleared
Dec 15, 1986
ARTHROSCOPIC SHOULDER LIGAMENT REPAIR KIT
Orthopedic
201d
Cleared
Sep 07, 1984
GUIDE TO THE KNEE
General & Plastic Surgery
30d
Cleared
Feb 27, 1984
MENISCAL SUTURING SYSTEM
Orthopedic
104d
Cleared
Nov 14, 1983
DISPOSABLE ARTHROSCOPY BLADE
Orthopedic
33d
Cleared
May 07, 1982
INTRA-ARTICULAR SURGICAL SYSTEM
Orthopedic
87d
Cleared
Sep 24, 1981
THE ARTHROFILE
General & Plastic Surgery
23d
Cleared
Apr 05, 1979
DYONICS STEROTOXIC POSITIONER
Neurology
23d
Cleared
Feb 01, 1978
INTRA-ARTICULAR SHAVER
Orthopedic
211d