Medical Device Manufacturer · US , Miami , FL

Symbiosis Corp. - FDA 510(k) Cleared Devices

34 submissions · 32 cleared · Since 1989

Total

Cleared

Denied

Symbiosis Corp. has 32 FDA 510(k) cleared medical devices. Based in Miami, US.

Historical record: 32 cleared submissions from 1989 to 1996. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Symbiosis Corp. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Symbiosis Corp.

34 devices

1-12 of 34

Cleared Jan 18, 1996

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES

K955119 · HIH

Obstetrics & Gynecology · 70d

Cleared Jan 17, 1996

SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES

K953453 · FAS

Gastroenterology & Urology · 182d

Cleared Oct 06, 1995

SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES

K953242 · KNF

Obstetrics & Gynecology · 87d

Cleared Jul 05, 1995

SYMBIOSIS BIPOLAR FORCEPS

K952432 · GEI

General & Plastic Surgery · 42d

Cleared Apr 10, 1995

SYMBIOSIS BIPOLAR SCISSORS

K951387 · GCJ

General & Plastic Surgery · 14d

Cleared Feb 03, 1995

SYMBIOSIS BIPOLAR SCISSORS

K950286 · GCJ

General & Plastic Surgery · 10d

Cleared Jan 20, 1995

SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS

K946238 · FCL

Gastroenterology & Urology · 29d

Cleared Jul 28, 1994

SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS

K930773 · HFB

Obstetrics & Gynecology · 527d

Cleared Jun 22, 1994

SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE

K941426 · GEI

General & Plastic Surgery · 90d

Cleared Mar 15, 1994

SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN

K932266 · KGE

Gastroenterology & Urology · 329d

Cleared Feb 28, 1994

SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS

K931957 · FCL

Gastroenterology & Urology · 314d

Cleared Dec 06, 1993

SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.

K924016 · HRX

Orthopedic · 482d

Symbiosis Corp. - FDA 510(k) Cleared Devices

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