Fibra Sonics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fibra Sonics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Fibra Sonics, Inc. has 10 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 10 cleared submissions from 1980 to 1999.
Browse the FDA 510(k) cleared devices submitted by Fibra Sonics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fibra Sonics, Inc.
10 devices
Cleared
Nov 22, 1999
FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000
Gastroenterology & Urology
73d
Cleared
Feb 17, 1999
EXONIX
Physical Medicine
85d
Cleared
Feb 16, 1999
FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM
Ophthalmic
90d
Cleared
Dec 14, 1998
FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 1000 CONSOLE MODEL
General & Plastic Surgery
91d
Cleared
Sep 22, 1998
FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA
General & Plastic Surgery
194d
Cleared
Dec 11, 1984
ULTRASONIC LITHOTRIPTOR 300A
Gastroenterology & Urology
207d
Cleared
Mar 16, 1984
PHACO FRAGMENTOR GT-1
Ophthalmic
88d
Cleared
Feb 04, 1982
ULTRASONIC FRAGMENTOR
Radiology
63d
Cleared
Dec 14, 1981
HYGIENTIST
Dental
56d
Cleared
Dec 17, 1980
LEWICKY ANTERIOR CHAMBER MAINTEN. SYS.
Ophthalmic
79d