Apatech, Ltd.

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Web: http://www.apatech.com
E-Mail:
Address: 327 Mile End Road, London E1 4NS, United Kingdom
Phone: +44-(0)-20-7882-7502 | Fax: +44-(0)-20-7882-7503 | Map/Directions >>

Profile: Apatech, Ltd. specializes in synthetic bone graft technologies. Our technology is based on initial research to engineer the optimum structure and chemistry for a safe, effective bone graft material that closely approximates natural bone, thus providing an osteoconductive scaffold for new bone growth. We provide products like actifuse granules, actifuse ABX, actifuse shape, actifuse microgranules & actifuse easyPrep. Our ApaPore™ is a synthetic & porous hydroxyapatite readily available & manufactured to a highly controlled specification, thus providing a cost-effective bone graft. Actifuse resorption is cell mediated and avoids a biological race between graft dissolution and new bone formation. This minimises the risk of a foreign body response to particulate debris observed with some synthetic materials.

17 Products/Services (Click for related suppliers)

• Absorbable Adhesion Barrier (FDA Code: MCN)

• Artificial Hydroxyapatite

• Artificial Hydroxyapatite Orbital Implant

• Bio-Eyes Hydroxyapatite Orbital Implant

• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)

A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.

• 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.

• Gas Cylinder Pressure Regulator (FDA Code: CAN / 868.2700)

A pressure regulator is a device, often called a pressure-reducing valve, that is intended for medical purposes and that is used to convert a medical gas pressure from a high variable pressure to a lower, more constant working pressure. This device includes mechanical oxygen regulators.

• General & Plastic Surgery Laparoscope (FDA Code: GCJ / 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.

• Heating Block (FDA Code: JRG / 862.2050)

General purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use.

• Hydroxyapatite

• Hydroxyapatite Coated Implants

• Hydroxyapatite Orbital Implants

• I.V. Fluid Transfer Unit (FDA Code: LHI / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Non Dental Irrigating Syringe (FDA Code: KYZ / 880.6960)

An irrigating syringe is a device intended for medical purposes that consists of a bulb or a piston syringe with an integral or a detachable tube. The device is used to irrigate, withdraw fluid from, or instill fluid into, a body cavity or wound.

• Piston Syringe (FDA Code: FMF / 880.5860)

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

• Polymerizing Sealant (FDA Code: NBE)

• Porous hydroxyapatite orbital implants