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Luxtec

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Web: http://www.luxtec.com
E-Mail:
Address: 99 Hartwell Street, West Boylston, Maryland 01583, USA
Phone: +1-(508)-835-9700 | Fax: +1-(508)-835-9976 | Map/Directions >>
 
 

Profile: Luxtec produces medical illumination systems. We develop lighting and visualization systems for the operating room. Our products include headlights, ultralite, halogen, camera, surgical loupes, monitors, printers, and light sources. Our ultralite consists of ergonomic designs that use the head's natural contours to hold the light in place without uncomfortable pressure. Our MicroLux® DLX headlight camera system gives an entirely new way to visualize, edit, share and store surgical cases. Our adjustable surgical loupes make fitting easy and simplify the customization procedure to a minor movement of the loupe body. It requires neither time-consuming multiple fittings nor intrusive Pupillary Distance (PD) measurements. The frames can be fitted with prescription lenses and adjusted to fit the surgeon's PD on the spot. Our light source brings the brilliance of surgical lighting with the breakthrough CLX system, which is the first Xenon light source designed specifically for private practice, surgical centers and community hospitals. We develop lighting and visualization systems for the operating room.

The company was founded in 1981, has revenues of USD 10-25 Million, has ~140 employees and is ISO 9001, CE certified. NASDAQ:IART (SEC Filings)

51 to 100 of 439 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 [2] 3 4 5 6 7 8 9 >> Next 50 Results
• Clip Removal Instrument (FDA Code: HBQ / 882.4200)
A clip removal instrument is a device used to remove surgical clips from the patient.
• Clip Surgical Applier (FDA Code: GDO / 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.
• Collagen Wound Dressing (FDA Code: KGN)
• Collagen-Based Absorbable Hemostatic Agent (FDA Code: LMF / 878.4490)
An absorbable hemostatic agent or dressing is a device intended to produce hemostasis by accelerating the clotting process of blood. It is absorbable.
• Continuous Intracranial Pressure Monitor (FDA Code: GWM / 882.1620)
An intracranial pressure monitoring device is a device used for short-term monitoring and recording of intracranial pressures and pressure trends. The device includes the transducer, monitor, and interconnecting hardware.
• Corneo-Scleral Punch (FDA Code: HNJ / 886.4350)
A manual ophthalmic surgical instrument is a nonpowered, handheld device intended to aid or perform ophthalmic surgical procedures. This generic type of device includes the manual corneal burr, ophthalmic caliper, ophthalmic cannula, eyelid clamp, ophthalmic muscle clamp, iris retractor clip, orbital compressor, ophthalmic curette, cystotome, orbital depressor, lachrymal dilator, erisophake, expressor, ophthalmic forcep, ophthalmic hook, sphere introducer, ophthalmic knife, ophthalmic suturing needle, lachrymal probe, trabeculotomy probe, cornea-sclera punch, ophthalmic retractor, ophthalmic ring (Flieringa), lachrymal sac rongeur, ophthalmic scissors, enucleating snare, ophthalmic spatula, ophthalmic specula, ophthalmic spoon, ophthalmic spud, trabeculotome or ophthalmic manual trephine.
• Cortical Electrode (FDA Code: GYC / 882.1310)
A cortical electrode is an electrode which is temporarily placed on the surface of the brain for stimulating the brain or recording the brain's electrical activity.
• Cryophthalmic Unit (FDA Code: HPS / 886.4170)
A cryophthalmic unit is a device that is a probe with a small tip that becomes extremely cold through the controlled use of a refrigerant or gas. The device may be AC-powered. The device is intended to remove cataracts by the formation of an adherent ice ball in the lens, to freeze the eye and adjunct parts for surgical removal of scars, and to freeze tumors.
• Cryosurgical Unit (FDA Code: GEH / 878.4350)
• Curettes (FDA Code: HTF / 878.4800)
• Cystotome (FDA Code: HNY / 886.4350)
• Depth Electrodes (FDA Code: GZL / 882.1330)
A depth electrode is an electrode used for temporary stimulation of, or recording electrical signals at, subsurface levels of the brain.
• Depth Gauge (FDA Code: HTJ / 888.4300)
A depth gauge for clinical use is a measuring device intended for various medical purposes, such as to determine the proper length of screws for fastening the ends of a fractured bone.
• Dermal Replacement Device (FDA Code: MDD)
• Dermatomes (FDA Code: GFD / 878.4820)
Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.
• Diagnostic/Surgical Loupe (FDA Code: FSP / 878.4800)
• Digital Video Recorders
• Disposable Aspiration and Injection Needle (FDA Code: GAA / 878.4800)
• Disposable Medical Scissors (FDA Code: JOK / 880.6820)
Medical disposable scissors are disposable type general cutting devices intended for medical purposes. This generic type of device does not include surgical scissors.
• Drill Bit (FDA Code: HTW / 888.4540)
An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.
• Drill Brace (FDA Code: HXY / 888.4540)
• Drill Handpiece (Brace) (FDA Code: HBD / 882.4325)
A cranial drill handpiece (brace) is a hand holder, which is used without a power source, for drills, burrs, trephines, or other cutting tools that are used on a patient's skull.
• Drug Wound Dressing (FDA Code: FRO)
• Dura-Substitute (FDA Code: GXQ / 882.5910)
A dura substitute is a sheet or material that is used to repair the dura mater (the membrane surrounding the brain).
• Ear Cannula (FDA Code: JYC / 878.4800)
• Ear Curette (FDA Code: JYG / 874.4420)
• Ear Excavator (FDA Code: JYH / 874.4420)
• Ear Knife (FDA Code: JYO / 874.4420)
• Ear Rasp (FDA Code: JYY / 874.4420)
• Ear Scissors (FDA Code: JZB / 874.4420)
• Ear Snare (FDA Code: JZD / 874.4420)
• Ear Speculum (FDA Code: EPY / 878.1800)
A speculum is a device intended to be inserted into a body cavity to aid observation. It is either nonilluminated or illuminated and may have various accessories.
• Ear Spoon (FDA Code: JZE / 874.4420)
• Ear Suction Tube (FDA Code: JZF / 874.4420)
• Ear-Lobe Perforator (FDA Code: JYS / 874.4420)
• Electrical-Powered Muscle Stimulator (FDA Code: IPF / 890.5850)
A powered muscle stimulator is an electrically powered device intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.
• Electrode Cables (FDA Code: IKD / 890.1175)
An electrode cable is a device composed of strands of insulated electrical conductors laid together around a central core and intended for medical purposes to connect an electrode from a patient to a diagnostic machine.
• Electrosurgical Cutting and Coagulation Device (FDA Code: GEI / 878.4400)
An electrosurgical cutting and coagulation device and accessories is a device intended to remove tissue and control bleeding by use of high-frequency electrical current.
• Emesis Basin (FDA Code: FNY / 880.6730)
A body waste receptacle is a device intended for medical purposes that is not attached to the body and that is used to collect the body wastes of a bed patient.
• Endometrial Suction Curette and Accessories (FDA Code: HHK / 884.1175)
An endometrial suction curette is a device used to remove material from the uterus and from the mucosal lining of the uterus by scraping and vacuum suction. This device is used to obtain tissue for biopsy or for menstrual extraction. This generic type of device may include catheters, syringes, and tissue filters or traps.
• Endoscope Accessories (FDA Code: KOG)
• Endoscopic Light Source
• Endoscopic Sponge Carrier (FDA Code: FGS / 876.1500)
An endoscope and accessories is a device used to provide access, illumination, and allow observation or manipulation of body cavities, hollow organs, and canals. The device consists of various rigid or flexible instruments that are inserted into body spaces and may include an optical system for conveying an image to the user's eye and their accessories may assist in gaining access or increase the versatility and augment the capabilities of the devices. Examples of devices that are within this generic type of device include cleaning accessories for endoscopes, photographic accessories for endoscopes, nonpowered anoscopes, binolcular attachments for endoscopes, pocket battery boxes, flexible or rigid choledochoscopes, colonoscopes, diagnostic cystoscopes, cystourethroscopes, enteroscopes, esophagogastroduodenoscopes, rigid esophagoscopes, fiberoptic illuminators for endoscopes, incandescent endoscope lamps, biliary pancreatoscopes, proctoscopes, resectoscopes, nephroscopes, sigmoidoscopes, ureteroscopes, urethroscopes, endomagnetic retrievers, cytology brushes for endoscopes, and lubricating jelly for transurethral surgical instruments. This section does not apply to endoscopes that have specialized uses in other medical specialty areas and that are covered by classification regulations in other parts of the device classification regulations.
• Endoscopic Video Camera
• ENT Applicator (FDA Code: KCJ / 874.5220)
An ear, nose, and throat drug administration device is one of a group of ear, nose, and throat devices intended specifically to administer medicinal substances to treat ear, nose, and throat disorders. These instruments include the powder blower, dropper, ear wick, manual nebulizer pump, and nasal inhaler.
• ENT Elevator (FDA Code: KAD / 874.4420)
• ENT Forceps (FDA Code: KAE / 874.4420)
• ENT Headlight
• ENT Irrigation Syringe (FDA Code: KCP / 874.5220)
• ENT Knife (FDA Code: KTG / 874.4420)

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