Aksioma, Inc.

Contact: Sophia Pesotchinsky
Address: 8 Chapygina Str., St. Petersburg 197376, Russian Federation | Map/Directions >>

Profile: Aksioma, Inc. deals with electric & non electric biopsy forceps and flexible stone dislodgers.

FDA Registration Number: 3004468438
US Agent: Sophiapesotchinsky / Lsvp International, Inc.
Phone: +1-(650)-969-1000 Fax: +1-(650)-969-2300 E-Mail:

3 Products/Services (Click for related suppliers)

• Electric Biopsy Forceps (FDA Code: KGE / 876.4300)

An endoscopic electrosurgical unit and accessories is a device used to perform electrosurgical procedures through an endoscope. This generic type of device includes the electrosurgical generator, patient plate, electric biopsy forceps, electrode, flexible snare, electrosurgical alarm system, electrosurgical power supply unit, electrical clamp, self-opening rigid snare, flexible suction coagulator electrode, patient return wristlet, contact jelly, adaptor to the cord for transurethral surgical instruments, the electric cord for transurethral surgical instruments, and the transurethral desiccator.

• Flexible Stone Dislodger (FDA Code: FGO / 876.4680)

A ureteral stone dislodger is a device that consists of a bougie or a catheter with an expandable wire basket near the tip, a special flexible tip, or other special construction. It is inserted through a cystoscope and used to entrap and remove stones from the ureter. This generic type of device includes the metal basket and the flexible ureteral stone dislodger.

• Non-Electric Biopsy Forceps (FDA Code: FCL / 876.1075)

A gastroenterology-urology biopsy instrument is a device used to remove, by cutting or aspiration, a specimen of tissue for microscopic examination. This generic type of device includes the biopsy punch, gastrointestinal mechanical biopsy instrument, suction biopsy instrument, gastro-urology biopsy needle and needle set, and nonelectric biopsy forceps. This section does not apply to biopsy instruments that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.