Symbiosis Corp.
Symbiosis Corp. holds FDA 510(k) medical device clearances, first cleared 1989, most recent 1996.
Top product codes for Symbiosis Corp.
Recent clearances by Symbiosis Corp.
- K955119 — SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
- K953453 — SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
- K953242 — SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
- K952432 — SYMBIOSIS BIPOLAR FORCEPS
- K951387 — SYMBIOSIS BIPOLAR SCISSORS
- K950286 — SYMBIOSIS BIPOLAR SCISSORS
- K946238 — SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
- K930773 — SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
- K941426 — SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
- K932266 — SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
- K931957 — SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPS
- K924016 — SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.
- K932265 — SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HAND
- K931793 — SYMBIOSIS ENT SURGICAL INSTRUMENTS
- K930160 — ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLE
- K930158 — BONE MARROW BIOPSY PROCEDURE TRAY
- K926109 — FLUID DRAINAGE TRAY
- K925707 — INSTRUMENT, MANUAL, GENERAL SURGICAL
- K924501 — GILLAM-TUKEL BONE MARROW BIOPSY NEEDLE
- K924017 — SYMBIOSIS DISPOSABLE ARTHROSCOPIC SURGICAL INST.
- K925410 — SYMBIOSIS HEMOSTATIC WAND
- K925416 — SYMBIOSIS BONE MARROW BIOPSY NEEDLE
- K924702 — TURKEL ABDOMINAL PARACENTESIS SYSTEM
- K923563 — SYMBIOSIS SUCTION-IRRIGATOR
- K920762 — BIOSPSY FORCEPS
- K922571 — INSTRUMENT, MANUAL, GENERAL SURGICAL
- K923028 — TURKEL PNEUMOTHORAX KIT
- K921461 — TURKEL THORACENTESIS NEEDLE
- K922614 — TURKEL THORACENTESIS SYSTEM
- K910831 — ENDOPATH SURGICAL INSTRUMENTS
- K910964 — HOT BIOPSY FORCEPS
- K910855 — ENDOPATH VERESS NEEDLE
- K895415 — BIOPSY FORCEPS
- K894419 — GASTRO ENTEROLOGICAL BIOPTOME
Data sourced from openFDA. This site is unofficial and independent of the FDA.