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Chattanooga Group


Web: http://www.chattgroup.com
Address: 4717 Adams Road, Hixson, Tennessee 37343, USA
Phone: +1-(423)-870.2281, 800.592.7329 | Map/Directions >>
 
 

Profile: Chattanooga Group produces rehabilitation equipment for treating skeletal, muscular, neurological and soft tissue disorders. Our laser therapy uses light to penetrate tissue for increased blood flow and more rapid healing. We also develop orthopedic devices. Our myossage® lotion gives a soothing, effective massage. It is alcohol-free, non-greasy and non-staining. Electrotherapy stimulates injured muscles and joints to activate the body's natural processes for relieving pain, building strength and promoting healing. The Intelect TranSport® line of portable therapy products is equally as adept on the go as it is in the clinic. Each unit's unique design allows it be to be used for tabletop, wall mount, therapy cart or mobile use. Its lightweight design, battery-powered option and custom carrying bag allows the user to conveniently use it.

The company was founded in 1947, has revenues of USD 50-100 Million, has ~300 employees and is ISO 9001, CE certified.

201 to 250 of 330 Products/Services (Click for related suppliers)  Page: << Previous 50 Results 1 2 3 4 [5] 6 7 >> Next 50 Results
• Non-ice Cold Packs
• Non-Invasive Traction Component (FDA Code: KQZ / 888.5890)
A noninvasive traction component is a device, such as a head halter, pelvic belt, or a traction splint, that does not penetrate the skin and is intended to assist in connecting a patient to a traction apparatus so that a therapeutic pulling force may be applied to the patient's body.
• Non-Measuring Passive Exerciser
• Non-Powered Dynamometer (FDA Code: HRW / 888.1250)
A nonpowered dynamometer is a mechanical device intended for medical purposes to measure the pinch and grip muscle strength of a patient's hand.
• Non-Powered Goniometer (FDA Code: KQW / 888.1520)
A nonpowered goniometer is a mechanical device intended for medical purposes to measure the range of motion of joints.
• Non-Powered Surgical Instrument (FDA Code: HAO / 882.4535)
A nonpowered neurosurgical instrument is a hand instrument or an accessory to a hand instrument used during neurosurgical procedures to cut, hold, or manipulate tissue. It includes specialized chisels, osteotomes, curettes, dissectors, elevators, forceps, gouges, hooks, surgical knives, rasps, scissors, separators, spatulas, spoons, blades, blade holders, blade breakers, probes, etc.
• Non-Powered Traction Apparatus (FDA Code: HST / 888.5850)
A nonpowered orthopedic traction apparatus is a device that consists of a rigid frame with nonpowered traction accessories, such as cords, pulleys, or weights, and that is intended to apply a therapeutic pulling force to the skeletal system.
• Orthopedic Burr (FDA Code: HTT / 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.
• Orthopedic Cushions
• Orthopedic Cutting Instrument (FDA Code: HTZ / 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.
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540)
• Osteophilic Finish Uncemented Semi- Hip Prosthesis (FDA Code: MBL / 888.3358)
A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.
• Pain Management System
• Paraffin Wax Bath
• Paraffin Wax Kits
• Patellofemorotibial Knee Prosthesis (FDA Code: MBH / 888.3565)
A knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device is designed to achieve biological fixation to bone without the use of bone cement. This identification includes fixed-bearing knee prostheses where the ultra high molecular weight polyethylene tibial bearing is rigidly secured to the metal tibial base plate.
• Patient Examination Gowns & Capes
• Patient Lifters (FDA Code: FNG / 880.5500)
An AC-powered lift is an electrically powered device either fixed or mobile, used to lift and transport patients in the horizontal or other required position from one place to another, as from a bed to a bath. The device includes straps and slings to support the patient.
• Patient Lifts and Accessories (FDA Code: FNG / 880.5500)
• Pediatric Exam Tables
• Pediatric Multipositioning Wheelchairs
• Pediatric Sport Wheelchairs
• Pediatric Wheelchairs
• Pelvic Traction Belt (FDA Code: HSQ / 888.5890)
• Pillow Contoured
• Pillows & Cushions
• Plinth (FDA Code: INT / 890.3520)
A plinth is a flat, padded board with legs that is intended for medical purposes. A patient is placed on the device for treatment or examination.
• Portable Paraffin Baths
• Portable Wheelchairs
• Positioning Systems, Foot Supports
• Positioning Systems, Head Supports
• Positioning Systems, Legrests
• Positioning Systems, Lumbar Supports
• Positioning Systems, Neck Supports
• Positioning Systems, Positioning Systems
• Positioning Systems, Shoulder Supports
• Post-Surgery Compression Garments
• Power Wheelchairs
• Powered Exerciser (FDA Code: BXB / 890.5380)
Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Examples include a powered treadmill, a powered bicycle, and powered parallel bars.
• Powered Heating Pad (FDA Code: IRT / 890.5740)
A powered heating pad is an electrical device intended for medical purposes that provides dry heat therapy for body surfaces. It is capable of maintaining an elevated temperature during use.
• Powered Heating Unit (FDA Code: IRQ / 890.5950)
A powered heating unit is a device intended for medical purposes that consists of an encased cabinet containing hot water and that is intended to heat and maintain hot packs at an elevated temperature.
• Powered Muscle Stimulator For Muscle Conditioning (FDA Code: NGX / 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.
• Powered Table (FDA Code: INQ / 890.3760)
A powered table is a device intended for medical purposes that is an electrically operated flat surface table that can be adjusted to various positions. It is used by patients with circulatory, neurological, or musculoskeletal conditions to increase tolerance to an upright or standing position.
• Powered Traction Equipment (FDA Code: ITH / 890.5900)
Powered traction equipment consists of powered devices intended for medical purposes for use in conjunction with traction accessories, such as belts and harnesses, to exert therapeutic pulling forces on the patient's body.
• Prone Pillows
• Prosthesis Driver (FDA Code: HWR / 888.4540)
• Reamer (FDA Code: HTO / 888.4540)
• Reclining Wheelchairs
• Reclining Wheelchairs & Accessories
• Rehab & Fitness Equipment

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