Symbiosis Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Symbiosis Corp. - FDA 510(k) Cleared Devices
34
Total
32
Cleared
0
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
Cleared
Jan 18, 1996
SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
Obstetrics & Gynecology
70d
Cleared
Jan 17, 1996
SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
Gastroenterology & Urology
182d
Cleared
Oct 06, 1995
SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
Obstetrics & Gynecology
87d
Cleared
Jul 05, 1995
SYMBIOSIS BIPOLAR FORCEPS
General & Plastic Surgery
42d
Cleared
Apr 10, 1995
SYMBIOSIS BIPOLAR SCISSORS
General & Plastic Surgery
14d
Cleared
Feb 03, 1995
SYMBIOSIS BIPOLAR SCISSORS
General & Plastic Surgery
10d
Cleared
Jan 20, 1995
SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
Gastroenterology & Urology
29d
Cleared
Jul 28, 1994
SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
Obstetrics & Gynecology
527d
Cleared
Jun 22, 1994
SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
General & Plastic Surgery
90d
Cleared
Mar 15, 1994
SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
Gastroenterology & Urology
329d
Cleared
Feb 28, 1994
SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS
Gastroenterology & Urology
314d
Cleared
Dec 06, 1993
SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.
Orthopedic
482d