Immunostics, Inc.

Address: 3505 Sunset Ave, Ocean, New Jersey 07712, USA
Phone: +1-(732)-918-0770 | Map/Directions >>

Profile: Immunostics, Inc. supplies colon cancer screening program using our hema screen test for fecal occult blood. We are one of the originators of fecal occult blood testing using Guaiac technology. We offer tests like pregnancy, immunological & serological & bacteriological. We provide rapid carbon & non-carbon assays & controls for the determination of syphilis including RPR carbon and syphilis control products. Our Hema Screen tm is a rapid, convenient, qualitative method for detecting asymptomatic occult bleeding.

The company was founded in 1983, has revenues of USD 1-5 Million, has ~30 employees.

FDA Registration Number: 2244821

42 Products/Services (Click for related suppliers)  
• Anti-Streptokinase Test (FDA Code: GTO / 866.3720)
• Antisera, Control for Non-Treponemal Test (FDA Code: GMP / 866.3820)
• Brucella Spp Agglutination Antigen (FDA Code: GSO / 866.3085)
• C-Reactive Protein Test System (FDA Code: DCN / 866.5270)
A C-reactive protein immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the C-reactive protein in serum and other body fluids. Measurement of C-reactive protein aids in evaluation of the amount of injury to body tissues.
• Chemistry Analyzers
• Clinical Immunochemistry Analyzers
• Controls
• CPR Equipment
• Febrile Antigen (FDA Code: GSZ / 866.3410)
• Febrile Antigens Slide/Tube Test (FDA Code: GNC / 866.3550)
• Fecal Occult Blood Test
• Fecal Occult Blood Test Kits
• Fecal Occult Blood Testing Kit
• Fertility Monitors, Pregnancy Test Kits
• Gastric and Fecal Occult Blood Test
• General Diagnostic Supplies
• General EMT
• General Examination Supplies
• General Medical Supplies
• HCG Over The Counter Pregnancy Test Kit (FDA Code: LCX / 862.1155)
A human chorionic gonadotropin (HCG) test system is a device intended for the early detection of pregnancy is intended to measure HCG, a placental hormone, in plasma or urine.
• Home pregnancy test kits, Hcg
• Human and Animal Sera (FDA Code: KIS / 864.2800)
Animal and human sera are biological products, obtained from the blood of humans or other animals, that provide the necessary growth-promoting nutrients in a cell culture system.
• Human Chorionic Gonadotropin Agglutination Method (FDA Code: JHJ / 862.1155)
• Human Chorionic Gonadotropin Radioimmunoassay (FDA Code: JHI / 862.1155)
• Human Chorionic Gonadotropin Test
• Immuno Chemistry Analyzers
• Immunoassay Equipment, Immunochemistry Analyzers
• Infectious Mononucleosis Test System (FDA Code: KTN / 866.5640)
An infectious mononucleosis immunological test system is a device that consists of the reagents used to measure by immunochemical techniques heterophile antibodies frequently associated with infectious mononucleosis in serum, plasma, and other body fluids. Measurements of these antibodies aid in the diagnosis of infectious mononucleosis.
• Non-Treponemal Antigen (FDA Code: GMQ / 866.3820)
• Occult Blood Reagent (FDA Code: KHE / 864.6550)
An occult blood test is a device used to detect occult blood in urine or feces. (Occult blood is blood present in such small quantities that it can be detected only by chemical tests of suspected material, or by microscopic or spectroscopic examination.)
• Positive and Negative Febrile Antigen Control Serum (FDA Code: GSN / 866.3085)
• Pregnancy Kits
• Pregnancy Test Kit
• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775)
A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis.
• Rubella Latex Agglutination Assay (FDA Code: LQN / 866.3510)
Rubella virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubella virus in serum. The identification aids in the diagnosis of rubella (German measles) or confirmation of a person's immune status from past infections or immunizations and provides epidemiological information on German measles. Newborns infected in the uterus with rubella virus may be born with multiple congenital defects (rubella syndrome).
• Salmonella Spp Antigen (FDA Code: GRL / 866.3550)
• Serum Human Chorionic Gonadotropin Test (FDA Code: DHA / 862.1155)
• Shigella Spp Antigen (FDA Code: LIA / 866.3660)
• Staphylococcus Aureus Protein A Insoluble (FDA Code: LHJ / 866.3700)
• Syphilis Test
• Systemic Lupus Erythematosus Test (FDA Code: DHC / 866.5820)
A systemic lupus erythematosus (SLE) immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum and other body fluids that react with cellular nuclear double-stranded deoxyribonucleic acid (DNA) or other nuclear constituents that are specifically diagnostic of SLE. Measurement of nuclear double-stranded DNA antibodies aids in the diagnosis of SLE (a multisystem autoimmune disease in which tissues are attacked by the person's own antibodies).
• Toxoplasma Gondii Direct Agglutination Test (FDA Code: LLA / 866.3780)

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