Medical Device Manufacturer · US , Walker , MI

Fibra Sonics, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1980

Total

Cleared

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

1-10 of 10

Cleared Nov 22, 1999

FIBRA SONICS ULTRASONIC LITHOTRIPTOR LITHOSONIC, MODEL LS-2000

K993046 · FEO

Gastroenterology & Urology · 73d

Cleared Feb 17, 1999

EXONIX

K984199 · IMI

Physical Medicine · 85d

Cleared Feb 16, 1999

FIBRA-SONICS PHACO III OR IIIP FRAGMENTATION SYSTEM

K984143 · HQC

Ophthalmic · 90d

Cleared Dec 14, 1998

FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 1000 CONSOLE MODEL

K983199 · LFL

General & Plastic Surgery · 91d

Cleared Sep 22, 1998

FIBRA SONICS ULTRASONIC SURGICAL ASPIRATOR SYSTEM, MODEL 2100 USSTA

K980930 · LFL

General & Plastic Surgery · 194d

Cleared Dec 11, 1984

ULTRASONIC LITHOTRIPTOR 300A

K842024 · FEO

Gastroenterology & Urology · 207d

Cleared Mar 16, 1984

PHACO FRAGMENTOR GT-1

K834453 · HQC

Ophthalmic · 88d

Cleared Feb 04, 1982

ULTRASONIC FRAGMENTOR

LEWICKY ANTERIOR CHAMBER MAINTEN. SYS.

K802381 · HQC

Ophthalmic · 79d

Fibra Sonics, Inc. - FDA 510(k) Cleared Devices

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