Heinz Kurz GmbH Medizintechnik

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Contact: Ms. Traute Kurz - Managing Dir.
Web: http://www.kurzmed.de
E-Mail:
Address: Tuebingerstr. 3, Dusslingen, BW D-72144, Germany
Phone: +49-(7072)-9179-0 | Fax: +49-(7072)-9179-79 | Map/Directions >>

Profile: Heinz Kurz GmbH Medizintechnik provides middle ear prostheses,nasal implants for rhinoplastic surgery,upper eyelid implants for oculoplasty,and ventilation tubes. ossicular replacement prosthesis. The angular ossicular replacement prosthesis plaster enables the integrity of the auditory ossicular chain to be restored in the event of destruction of the distal end of the long process of the incus. The two titanium bands play the role of a clamp and are attached to the incus. The bell fits onto the stapes capitulum. The pure mechanical connection of the titanium bands with the incus is very stable.

The company was founded in 1982, has revenues of USD 1-5 Million, has ~20 employees and is ISO 9001, CE certified.

FDA Registration Number: 8010617
US Agent: Wes Baker / Kurz Medical, Inc.
Phone: +1-(770)-349-6330 Fax: +1-(770)-934-3884 E-Mail:

13 Products/Services (Click for related suppliers)

• ENT Forceps (FDA Code: KAE / 874.4420)

• ENT Manual Surgical Instrument (FDA Code: LRC / 874.4420)

• ENT Surgical Tray (FDA Code: MMO / 874.4420)

• ENT Synthetic Polyamide Polymer (FDA Code: KHJ / 874.3620)

Ear, nose, and throat synthetic polymer material is a device material that is intended to be implanted for use as a space-occupying substance in the reconstructive surgery of the head and neck. The device is used, for example, in augmentation rhinoplasty and in tissue defect closures in the esophagus. The device is shaped and formed by the suregon to conform to the patient's needs. This generic type of device is made of material such as polyamide mesh or foil and porous polyethylene.

• External Eyelid Weights (FDA Code: MML / 886.5700)

• Incus and Stapes Ossicular Prosthesis

• Measuring Gauge (FDA Code: JYJ / 874.4420)

• Non-Sterile Prosthesis Modification For Ossicular Replacement Surgery Instrument (FDA Code: NNS / 874.3540)

A prosthesis modification instrument for ossicular replacement surgery is a device intended for use by a surgeon to construct ossicular replacements. This generic type of device includes the ear, nose, and throat cutting block; wire crimper, wire bending die; wire closure forceps; piston cutting jib; gelfoamTMpunch; wire cutting scissors; and ossicular finger vise.

• Partial Ossicular Replacement Prosthesis (FDA Code: ETB / 874.3450)

A partial ossicular replacement prosthesis is a device intended to be implanted for the functional reconstruction of segments of the ossicular chain and facilitates the conduction of sound wave from the tympanic membrane to the inner ear. The device is made of materials such as stainless steel, tantalum, polytetrafluoroethylene, polyethylene, polytetrafluoroethylene with carbon fibers composite, absorbable gelatin material, porous polyethylene, or from a combination of these materials.

• Scalpel Blade (FDA Code: GES / 878.4800)

A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• Surgical Cutter (FDA Code: FZT / 878.4800)

• Total Ossicular Replacement Prosthesis (FDA Code: ETA / 874.3495)

A total ossicular replacement prosthesis is a device intended to be implanted for the total functional reconstruction of the ossicular chain and facilitates the conduction of sound waves from the tympanic membrance to the inner ear. The device is made of materials such as polytetrafluoroethylene, polytetrafluoroethylene with vitreous carbon fibers composite, porous polyethylene, or from a combination of these materials.

• Tympanostomy Tube (FDA Code: ETD / 874.3880)

A tympanostomy tube is a device that is intended to be implanted for ventilation or drainage of the middle ear. The device is inserted through the tympanic membrane to permit a free exchange of air between the outer ear and middle ear. A type of tympanostomy tube known as the malleous clip tube attaches to the malleous to provide middle ear ventilation. The device is made of materials such as polytetrafluoroethylene, polyethylene, silicon elastomer, or porous polyethylene.