3by Ltd.

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Contact: David Lennarz
Web: http://www.3by.com
E-Mail:
Address: P.O.B. 65 Industrial Park Tefen, Tefen 24959, Israel
Phone: +972-(4)-9872332 | Fax: +972-(4)-9872340 | Map/Directions >>

Profile: 3by Ltd. specializes in turn-key projects of medical components, devices and systems. We provide clean room production, sophisticated plastic injection molding services, technical design assistance, assembly and product testing. Our solutions include injection, automatic assembly, product testing and automated packaging. We develop ampoule breaker that fits all ampoule sizes, eases the breakage of the cap and firmly grasps the cap for safe disposal. Our clean room production floor is ideal for the production of medical devices, moving from small quantities at the beginning of the development stage to large scale production.

The company is ISO 9001:2000 certified.

FDA Registration Number: 3004201393
US Agent: David Lennarz / Registrar Corp.
Phone: +1-(757)-224-0177 Fax: +1-(757)-224-0179 E-Mail:

26 Products/Services (Click for related suppliers)

• Ampule

• Arthroscopes (FDA Code: HRX / 888.1100)

An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.

• Bone Fixation Nail (FDA Code: JDS / 888.3030)

Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Contract Injection Molding

• Contract Manufacturing

• Embolectomy Catheters (FDA Code: DXE / 870.5150)

An embolectomy catheter is a balloon-tipped catheter that is used to remove thromboemboli, i.e., blood clots which have migrated in blood vessels from one site in the vascular tree to another.

• Endoscope Accessories (FDA Code: KOG)

• Engineering/Design Service

• Equipment Testing Services

• 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.

• Implantable Staple (FDA Code: GDW / 878.4750)

An implantable staple is a staple-like device intended to connect internal tissues to aid healing. It is not absorbable.

• Injection Molded Parts

• Intramedullary Fixation Rod and Accessories (FDA Code: HSB / 888.3020)

An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.

• Medical Devices

• Metal/Polymer Femoral Hemi- Hip Prosthesis (FDA Code: KWY / 888.3390)

A hip joint femoral (hemi-hip) metal/polymer cemented or uncemented prosthesis is a two-part device intended to be implanted to replace the head and neck of the femur. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a snap-fit acetabular component made of an alloy, such as cobalt-chromium-molybdenum, and ultra-high molecular weight polyethylene. This generic type of device may be fixed to the bone with bone cement (888.3027) or implanted by impaction.

• Needle Introducer & Knot Pusher

• Needles

• Packaging

• Plastics Injection Molding

• Polymeric Surgical Mesh (FDA Code: FTL / 878.3300)

Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.

• Product Design & Development

• Protoype Assembly Service

• Quality Assurance & Control

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Tamps (FDA Code: HXG / 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.

• Vertebroplasty Bone Cement (FDA Code: NDN / 888.3027)

Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.