Profile: Wampole Laboratories, a wholly owned subsidiary of Inverness Medical Inc., provides diagnostic testing & automation solutions for the clinical laboratory & point-of-care markets. Our full product line includes brands such as the AtheNA Multi-Lyte® test systems for clinical diagnostic testing and clearview point-of-care tests. We face the challenges by today's clinical laboratory and are dedicated to providing accurate and cost-effective diagnostic solutions across a broad test menu including autoimmune, infectious and enteric diseases, STDs, bladder cancer and cardiac risk. From technologically advanced platforms like the AtheNA Multi-Lyter Test system, a breakthrough in simultaneous, single-well, multiple-analyte testing, to one of the industry's most extensive selections of ELISA, IFA, serology and gel diffusion test kits and automation, we offers a full line of products and services to meet your laboratory's clinical diagnostics needs.

The company was founded in 2002, has revenues of USD 10-25 Million, has ~80 employees.

FDA Registration Number: 9710052
US Agent: Golden Jackie / Avo Dental Supplies Llc D/b/a Goldendent Llc
Phone: +1-(586)-585-1210  E-Mail: jgoldengolden-dent.com

51 to 100 of 110 Products/Services (Click for related suppliers)  Page: 1 [2] 3

• Herpes Simplex Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LGC / 866.3305)

• Herpes Virus Antibody

• Home pregnancy test kits, Hcg

• Human Chorionic Gonadotropin (hCG)

• Human Chorionic Gonadotropin (HCG) ELISA Kit

• Human Chorionic Gonadotropin (hCG) Enzyme Immunoassay Test Kit

• Human Chorionic Gonadotropin Agglutination Method (FDA Code: JHJ / 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.

• Human Prostate Specific Antigen, ELISA Test Kit

• Immuno Chemistry Analyzers

• Immunoassay Equipment, Immunochemistry Analyzers

• Immunoassay Reagents & Test Kits

• Immunoassays

• Indirect Immunofluorescent Anti-Smooth Muscle Antibody Test (FDA Code: DBE / 866.5120) An antismooth muscle antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the antismooth muscle antibodies (antibodies to nonstriated, involuntary muscle) in serum. The measurements aid in the diagnosis of chronic hepatitis (inflammation of the liver) and autoimmune connective tissue diseases (diseases resulting from antibodies produced against the body's own tissues).

• Indirect Immunofluorescent Anti-Thyroid Antibody

• Indirect Immunofluorescent Multiple Auto Antibody (FDA Code: DBL / 866.5660) A multiple autoantibodies immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoantibodies (antibodies produced against the body's own tissues) in serum and other body fluids. Measurement of multiple autoantibodies aids in the diagnosis of autoimmune disorders (disease produced when the body's own tissues are injured by autoantibodies).

• Infectious Disease Exams

• Infectious Disease Identification Test Kits

• Infectious Disease Test Kits

• Infectious Disease Testing, Rotavirus Test Kits

• 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.

• Instruments, Immunoassays

• Legionella (L. pneumophilia) Test Kits

• Legionella Spp. ELISA (FDA Code: MJH / 866.3300)

• Lyme Disease (Borrelia) Test Kits

• Lyme Disease Test

• Measles (Rubeola) and Mumps Test Kits

• Microbiology Identification Test Kits

• Microbiology Kit

• Mononucleosis Antibody (MONO) Test Kits

• Mumps Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LJY / 866.3380) Mumps virus serological reagents consist of antigens and antisera used in serological tests to identify antibodies to mumps virus in serum. Additionally, some of these reagents consist of antisera conjugated with a fluorescent dye (immunofluorescent reagents) used in serological tests to identify mumps viruses from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of mumps and provides epidemiological information on mumps. Mumps is an acute contagious disease, particularly in children, characterized by an enlargement of one or both of the parotid glands (glands situated near the ear), although other organs may also be involved.

• Mycoplasma Spp Enzyme Linked Immunoabsorbent Assay (FDA Code: LJZ / 866.3375)

• POC Rapid Cardiac Markers

• Pregnancy Kits

• Pregnancy Test Kit

• Pregnancy Testing Kits

• Prostate Specific Antigen Semi-Quantitative Rapid Test Strip

• Prostate Specific Antigen Testing kit

• PSA Prostate Specific Antigen IRMA 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.

• Rotavirus Test Kits

• Rotavirus Test, Gastroenteritis

• Rubella and Torch Test Kits

• Rubella Enzyme Linked Immunoabsorbent Assay (FDA Code: LFX / 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).

• Rubella HA Antigen (FDA Code: GOL / 866.3510)

• Rubeola Enzyme Linked Immunoabsorbent Assay (FDA Code: LJB / 866.3520) Rubeola (measles) virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubeola virus in serum. The identification aids in the diagnosis of measles and provides epidemiological information on the disease. Measles is an acute, highly infectious disease of the respiratory and reticuloendothelial tissues, particularly in children, characterized by a confluent and blotchy rash.

• Sensitive Pregnancy Tests

• Specialty Diagnostic Supplies

• Streptococcus Spp Antideoxyribonuclease (FDA Code: GTR / 866.3720)

• Streptococcus Test Kits

• Streptolysin O/Antistreptolysin-Titer Reagent