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Canica Design Inc.

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Contact: Julia Barry
Web: http://www.canica.com
E-Mail:
Address: 36 Mill Street, Almonte, Ontario K0A 1A0, Canada
Phone: +1-(613)-256-0350, 800-705-8312 | Fax: +1-(613)-256-0360 | Map/Directions >>
 
 

Profile: Canica Design Inc. is a medical device company that specializes in designing devices for the mechanical manipulation of soft tissues for use in acute care and chronic care settings. We develop a wide range of dynamic wound closure and stabilization devices, distributed internationally. ABRA® abdominal wall closure provides full fascia and skin closure, leaving nothing behind except a sound primary repair. The ABRA® abdominal wall closure system restores the primary closure option for full thickness and retracted midline abdominal defects. Over time, this dynamic wound closure system pulls the muscle planes together under tolerable tension while leaving fascial margins intact and ready to suture for a sound primary closure. This ABRA system eliminates the hernia without the need for mesh and re-approximates the skin margins, eliminating the need to graft. DynaClose™ provides an easy, painless and non-invasive method to close retracted or dehisced wounds up to 5 cm in width. DynaClose provides a second chance at skin closure for failing wounds or wounds under tension. DynaClose dynamic skin closure is indicated when retracted or dehisced wounds cannot be immediately reapproximated, when closed wounds are at risk of dehiscing, or when reduction of wound area under management is desirable. DynaStretch® is a non-invasive, topically applied adhesive-based device that stretches skin prior to a surgical intervention, creating a depot of skin that allows a primary closure after defect excision. It is indicated whenever a skin defect that is to be surgically removed is large enough that the resulting wound may not be primarily closeable under tolerable tension.

The company was founded in 1998.

9 Products/Services (Click for related suppliers)  
• Blood Collection Lancet (FDA Code: FMK / 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.
• General Surgical Manual Instrument (FDA Code: MDM / 878.4800)
• One-Piece Scalpel (FDA Code: GDX / 878.4800)
• Orthopedic Manual Surgical Instrument (FDA Code: LXH / 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.
• Removable Skin Clip (FDA Code: FZQ / 878.4320)
A removable skin clip is a clip-like device intended to connect skin tissues temporarily to aid healing. It is not absorbable.
• Scalpel Handle (FDA Code: GDZ / 878.4800)
• Skin Closure System (FDA Code: MKY / 878.4320)
• Suture Retention Device (FDA Code: KGS / 878.4930)
A suture retention device is a device, such as a retention bridge, a surgical button, or a suture bolster, intended to aid wound healing by distributing suture tension over a larger area in the patient.
• Topical Approximation System (FDA Code: MZR / 880.5240)
A medical adhesive tape or adhesive bandage is a device intended for medical purposes that consists of a strip of fabric material or plastic, coated on one side with an adhesive, and may include a pad of surgical dressing without a disinfectant. The device is used to cover and protect wounds, to hold together the skin edges of a wound, to support an injured part of the body, or to secure objects to the skin.

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