Bivona Medical Technologies - FDA 510(k) Cleared Devices
50
Total
50
Cleared
0
Denied
Bivona Medical Technologies has 50 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 50 cleared submissions from 1978 to 1995. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Bivona Medical Technologies Filter by specialty or product code using the sidebar.
50 devices
Cleared
Oct 31, 1995
SUPERSLICK
Anesthesiology
140d
Cleared
Oct 27, 1995
BURGET NASAL STENT
Ear, Nose, Throat
549d
Cleared
Oct 27, 1994
BIVONA FLEXTEND PEDIATRIC & NEONATAL TRACHEOSTROMY TUBES
Anesthesiology
62d
Cleared
Jul 01, 1994
BIVONA NASAL TURBINATE STENT
Ear, Nose, Throat
253d
Cleared
Oct 06, 1993
BIVONA ILLUMINATED ENDOTRACHEAL TUBE
Anesthesiology
86d
Cleared
Aug 10, 1993
BIVONA(R) ICU ENDOTRACHEAL TUBE
Anesthesiology
124d
Cleared
Jan 07, 1993
BIVONA HYPERFLEX TRACHEOSTOMY TUBE
Anesthesiology
220d
Cleared
Dec 29, 1992
BIVONA CUSTOMIZED TRACHEOSTOMY TUBES
Anesthesiology
148d
Cleared
Jul 27, 1992
BIVONA TRACHEAL T-TUBE STENT
Anesthesiology
167d
Cleared
Jun 29, 1992
BIVONA-COLORADO VOICE PROSTHESIS
Ear, Nose, Throat
188d
Cleared
Feb 03, 1992
BIVONA SLEEP APNEA TUBE
Anesthesiology
41d
Cleared
Jan 30, 1992
BIVONA FOME-CUF(R) & AIR CUF(R), MODIFICATION
Anesthesiology
156d
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