Profile: Seecor, Inc. specializes in providing esophageal pacing systems, fibrillators and foot prosthesis.
The company was founded in 1975, has revenues of < USD 1 Million.
9 Products/Services (Click for related suppliers)
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| • AC-Powered Fibrillator (FDA Code: LIW) |
| • Esophageal Pacing System (FDA Code: LPA) |
| • External Pacemaker Pulse Generator (FDA Code: DTE / 870.3600) An external pacemaker pulse generator is a device that has a power supply and electronic circuits that produce a periodic electrical pulse to stimulate the heart. This device, which is used outside the body, is used as a temporary substitute for the heart's intrinsic pacing sytem until a permanent pacemaker can be implanted, or to control irregular heartbeats in patients following cardiac surgery or a myocardial infarction. The device may have adjustments for impulse strength, duration, R-wave sensitivity, and other pacing variables. |
| • Fibrillator |
| • Flat Foot Prosthesis Fragment Sets |
| • Foot Prosthesis |
| • His Bundle Detector |
| • Metal/Polymer Semi-Constrained Ankle Prosthesis (FDA Code: HSN / 888.3110) An ankle joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace an ankle joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces and has no linkage across-the-joint. This generic type of device includes prostheses that have a talar resurfacing component made of alloys, such as cobalt-chromium-molybdenum, and a tibial resurfacing component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027). |
| • Other Catheter |