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Dave, NJ

Bharat Dave, Howell, NJ US

Patent application numberDescriptionPublished
20100284688APPARATUS AND METHOD FOR ENSURING CONTINUITY OF FIBER OPTIC - In a fiber-optic communications system, a backup or redundant optical link is provided at the central office in parallel with the primary one in use. Parameters associated with the backup link, including its signal delay, its attenuation, etc. are stored at the time of installation. Upon failure of the primary link, switchover can be automatic, and the stored parameters are used to make adjustments necessary for the differences between the primary link and the backup link. In addition, having information on the differences between the two links, the central office is able to send control information downstream which is used at the remote site to control changes that must be made for upstream signals. For example, customer equipment can be signaled to adjust its timing for the next time slot or interface amplifiers can be adjusted to account for the change in attenuation. The central office could be provided with a corrected interface to accommodate the new link and a substantial buffer to account for the change in timing, and switchover to the new timing could be done gracefully.11-11-2010

Ghanshyam Dave, Marlton, NJ US

Patent application numberDescriptionPublished
20100002588Network Switch With Onboard Diagnostics and Statistics Collection - The network switch is configured to enable monitoring of switched data. The network switch includes a housing and one or more port cards. Each port card has one or more physical ports and includes switching circuitry to selectively create a communication path between two physical ports. The network switch also includes packet analyzer circuitry, situated within the housing, to monitor data packets switched via a communication path between two physical ports without substantially degrading signal integrity of the data packets.01-07-2010

Kaushik J. Dave, Edison, NJ US

Patent application numberDescriptionPublished
20080227693Cyclic Peptide Isolation by Spray Drying - Methods for isolation of a synthetic cyclic peptide by spray drying, including spray drying at elevated temperatures, products made by the methods, and synthetic cyclic peptides preparations with defined characteristics, including an essentially amorphous acid addition salt of Ac-Nle-cyclo(-Asp-His-D-Phe-Arg-Trp-Lys)-OH in the form of a fine powder with a particle diameter of about 2 to about 20 microns.09-18-2008

Rajesh Dave, Short Hill, NJ US

Patent application numberDescriptionPublished
20090293719FRACTAL STRUCTURED NANOAGGLOMERATES AS FILTER MEDIA - Systems and methods for achieving filtration are provided that utilize agglomerates or granules of nanoparticles. The agglomerates or granules of nanoparticles may be used as and/or incorporated into a HEPA filtration system to remove solid or liquid submicron-sized particles, e.g., MPPS, in an efficient and efficacious manner. The filtration systems and methods are provided that utilize agglomerates or granules in a size range of about 100-500 microns. The agglomerates or granules of nanoparticles exhibit a hierarchical fractal structure. In the case of agglomerates of nanoparticles, porosities of 0.9 or greater are generally employed, and for granules of nanoparticles, porosities that are smaller than 0.9 may be employed. Filter media formed from the agglomerates or granules may be formed from materials such as carbon black and fumed silica, and may be employed in baffled or non-baffled filtration apparatus.12-03-2009

Rajesh N. Dave, Princeton, NJ US

Patent application numberDescriptionPublished
20090320588SYSTEM AND METHOD FOR MEASURING OR CHARACTERIZING PROPERTIES OF ULTRA-FINE OR COHESIVE POWDERS USING VIBRATIONS - The present disclosure provides for systems and methods for measuring and/or characterizing properties of ultra-fine or cohesive powders. More particularly, the present disclosure provides for systems and methods for measuring and/or characterizing packing density and/or flowability of ultra-fine or cohesive powders using vibrations. In one embodiment, the present disclosure provides for systems and methods for improved characterization or specification of powder or packing density as a function of consolidation stress. In an exemplary embodiment, the present disclosure also provides for systems and methods for improved characterization or definition of a parameter which indicates the flow property of the powder.12-31-2009

Vipul Bhupendra Dave, Hillsborough, NJ US

Patent application numberDescriptionPublished
20080226693Apparatus and Method for Making a Polymeric Structure - The apparatus and method for preparing a polymeric structure from which a number of medical devices may be constructed is described. The structures are preferably formed from bioabsorbable materials using low temperature fabrication processes, whereby drugs or other bio-active agents are incorporated into or onto the device and degradation of the drugs or other agents during processing is minimized. The method includes preparing a solution of at least one bioabsorbable polymer and a solvent. The solution is then deposited onto a stage and converted into a structure. The solvent is evaporated from the structure. The dried solution forms a structure that is removed from the stage and further dried before being stored in an inert environment. Thereafter, a medical device such as a stent may be constructed from the structure.09-18-2008
20090024202CEA SYSTEM AND METHOD FOR DELIVERING A SELF-EXPANDING STENT - Self-expanding stent delivery systems and methods having an introducer that receives a delivery catheter. The delivery catheter includes an outer body, an inner body and a stent loaded onto a stent bed within the inner body. The outer body receives the inner body with the stent loaded on the stent bed thereof. The outer body helps constrain the stent in its undeployed state in the stent bed until the stent is deployed by retraction of the outer body of the delivery catheter when the stent is identified as positioned across an intended treatment site. At least one anchoring mechanism provided on the inner body helps maintain the undeployed loaded stent appropriately in the stent bed during deployment. The at least one anchoring mechanism can include radiopaque material to increase fluoroscopic visualization of the stent during deployment, and the self-expanding stent can be a bio-absorbable material including drugs or other bio-active agents incorporated therein or provided thereon. The at least one anchoring mechanism can instead comprise a set of at least two bumpers between which the stent is loaded until deployed by retraction of the outer body of the delivery catheter when the stent has been appropriately positioned across an intended treatment site. After deployment of the stent at the intended treatment site, removal of the inner body and outer body of the delivery catheter and of the introducer occurs. Reliable and accurate emplacement of the stent across an intended treatment site is rendered more likely as a result.01-22-2009
20090026650METHOD OF FORMING A BIOABSORBABLE DRUG DELIVERY DEVICES - A bioabsorbable drug delivery device and various methods of making the same. The devices are preferably formed from bioabsorbable materials using low temperature fabrication processes, whereby drugs or other bio-active agents are incorporated into or onto the device and degradation of the drugs or other agents during processing is minimized. Radiopaque markers may also be incorporated into, or onto, the devices. The devices may be generally tubular helical stents comprised of a solid ladder or an open lattice configuration, or a hybrid combination thereof. The tubular helical stents are generally formed from precursor fibers, films or tubes. The solid ladder configuration provides increased radiopacity and increased radial strength, whereas the open lattice configuration provides better endothelialization and fluid flow through the stent. The drug or other agent delivery capacity of the devices may provide local or regionalized drug or other agent delivery, or a combination thereof, with more consistent concentrations of drugs or other agents delivered from the device to the treatment site along the entire length of the device.01-29-2009
20090148492METHOD OF MAKING A VASCULAR CLOSURE DEVICE - A method of making a biocompatible, implantable medical device, including a vascular closure device is disclosed. The method includes forming a biocompatible polymer into at least one fiber and randomly orienting the at least one fiber into a fibrous structure having at least one interstitial spaces. Polymeric materials may be utilized to fabricate any of these devices. The polymeric materials may include additives such as drugs or other bioactive agents as well as antibacterial agents. In such instances, at least one agent, in therapeutic dosage, is incorporated into at least one of the fibrous structure and the at least one fiber.06-11-2009
20090171388VASCULAR CLOSURE DEVICE - A biocompatible material may be configured into any number of implantable medical devices including a vascular closure device. The vascular closure device includes a fibrous structure formed from at least one randomly oriented fiber, the randomly oriented fiber comprising at least one polymer, and at least one agent, in therapeutic dosage, incorporated into at least one of the fibrous structure and the at least one randomly oriented fiber.07-02-2009
20090318955VASCULAR CLOSURE DEVICE - The present invention provides a porous structure that works very effectively to seal a puncture site with optimum porosity, absorbent capacity and perfect anatomical fit. The plug density and other fiber properties/geometry (total denier; number of filaments; etc) have provided an efficient structure that allows instantaneous absorption of blood during deployment. The final size of the plug with absorbed fluids provides an anatomical fit and seals the puncture site within few minutes after deployment.12-24-2009
20100280600DUAL DRUG STENT - Implantable medical devices may be utilized to locally delivery one or more drugs or therapeutic agents to treat a wide variety of conditions, including the treatment of the biological organism's reaction to the introduction of the implantable medical device. These therapeutic agents may be released under controlled and directional conditions so that the one or more therapeutic agents reach the correct target area, for example, the surrounding tissue and/or the bloodstream.11-04-2010

Patent applications by Vipul Bhupendra Dave, Hillsborough, NJ US