Profile: Inova Diagnostics, Inc. specializes in autoimmune disease diagnostics. We offer products like QUANTA LiteT (ELISA), NOVA LiteT(IFA), NOVA GELT(Ouchterlony), QUANTA PlexT (Luminexr), QUANTA ChekT (QC Panels) & specialty substrate slides. Our Quanta Lite™ ANA is an enzyme-linked immunosorbent assay (elisa) for the semi-quantitative detection of anti-nuclear antibodies (ANA) in human serum. Our Quanta Lite™ histone is an enzyme-linked immunosorbent assay (elisa) for the semi-quantitative detection of histone antibodies in human serum.

The company was founded in 1987, has revenues of USD 10-25 Million.

FDA Registration Number: 2026994

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• Alpha-Fetoprotein Rapid Test Strip

• Amphetamine Test Strip

• ANA (Antinuclear antibodies)

• Anaerotestr Test Strips

• Anti-Cyclic Citrullinated Peptide (Ccp) Antibodies (FDA Code: NHX / 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.

• Anti-Ribonucleic Acid Polymerase (Rnap) Iii Antibody Autoantibodies (FDA Code: NYO / 866.5100) An antinuclear antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the autoimmune antibodies in serum, other body fluids, and tissues that react with cellular nuclear constituents (molecules present in the nucleus of a cell, such as ribonucleic acid, deoxyribonucleic acid, or nuclear proteins). The measurements aid in the diagnosis of systemic lupus erythematosus (a multisystem autoimmune disease in which antibodies attack the victim's own tissues), hepatitis (a liver disease), rheumatoid arthritis, Sjogren's syndrome (arthritis with inflammation of the eye, eyelid, and salivary glands), and systemic sclerosis (chronic hardening and shrinking of many body tissues).

• Anti-Ribosomal P Antibodies (FDA Code: MQA / 866.5100)

• Anti-Smooth Muscle Anti-Actin Antibodies (FDA Code: NJF / 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).

• Anti-Ss-A 52 Autoantibodies (FDA Code: OBE / 866.5100)

• Antibodies to Glomerular Basement Membrane (gbm) Measure Devices (FDA Code: MVJ / 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).

• Antigen And Control Extractable Antinuclear Antibody (FDA Code: LLL / 866.5100)

• Antineutrophil Cytoplasmic Antibodies (ANCA) Test System (FDA Code: MOB / 866.5660)

• Antinuclear Antibody, Indirect Immunofluorescen (FDA Code: DHN / 866.5100)

• Antiparietal Cell Antibody Antigen Control, Enzyme Immunoassay (FDA Code: MLE / 866.5110) An antiparietal antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the specific antibody for gastric parietal cells in serum and other body fluids. Gastric parietal cells are those cells located in the stomach that produce a protein that enables vitamin B12to be absorbed by the body. The measurements aid in the diagnosis of vitamin B12deficiency (or pernicious anemia), atrophic gastritis (inflammation of the stomach), and autoimmune connective tissue diseases (diseases resulting when the body produces antibodies against its own tissues).

• Autoimmune Hepatitis Anti-Soluble Liver Antigen (Sla) Autoantibodies (FDA Code: NIY / 866.5660)

• Autoimmune Test Kits

• B2 - Glycoprotein I Antibodies Test System (FDA Code: MSV / 866.5660)

• Benzodiazepines Test Strip

• Blood Glucose Test Strips

• Blood Leak Test Strips

• Campylobacter Pylori (FDA Code: LYR / 866.3110)

• Carcinoembryonic Antigen Rapid Test Strip

• Centromere ELISA Kit

• Cholesterol Test Strips

• Chromatin ELISA Kit

• Coagulation Test Kits

• Cocaine Test Strip

• Complement C1q (FDA Code: DAK / 866.5240) A complement components immunological test system is a device that consists of the reagents used to measure by immunochemical techniques complement components C1q, C1r, C1s, C2, C3, C4, C5, C6, C7, C8, and C9, in serum, other body fluids, and tissues. Complement is a group of serum proteins which destroy infectious agents. Measurements of these proteins aids in the diagnosis of immunologic disorders, especially those associated with deficiencies of complement components.

• Control Antigen Antinuclear Antibody (FDA Code: LKJ / 866.5100)

• Creatinine Test Strips

• Diabetes Test Strips

• Diagnostic Test Kits

• Dry Reagent Test Strips

• Endomysial Autoantibodies (FDA Code: MVM / 866.5660)

• Enzyme Labeled Anti-DNA Antibody (FDA Code: LRM / 866.5100)

• Enzyme Labeled Antinuclear Antibody (FDA Code: LJM / 866.5100)

• Fecal Occult Blood Test Strip

• Flow Cytometry

• Flow Cytometry Test Kits

• Gliadin Antibodies (FDA Code: MST / 866.5750) A radioallergosorbent immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the allergen antibodies (antibodies which cause an allergic reaction) specific for a given allergen. Measurement of specific allergen antibodies may aid in the diagnosis of asthma, allergies, and other pulmonary disorders.

• Glutaraldehyde Test Strips

• Hcg Pregnancy Test Strip

• Histone ELISA Kit

• IgE Control (FDA Code: DGC / 866.5510) An immunoglobulins A, G, M, D, and E immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the immunoglobulins A, G, M, D, an E (serum antibodies) in serum. Measurement of these immunoglobulins aids in the diagnosis of abnormal protein metabolism and the body's lack of ability to resist infectious agents.

• Immunofluorescent Slide Processor

• Immunological Anticardiolipin Test System (FDA Code: MID / 866.5660)

• Indirect Immunofluorescent Anti-Smooth Muscle Antibody Test (FDA Code: DBE / 866.5120)

• Indirect Immunofluorescent Antimitochondrial Antibody Test (FDA Code: DBM / 866.5090) An antimitochondrial antibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the antimitochondrial antibodies in human serum. The measurements aid in the diagnosis of diseases that produce a spectrum of autoantibodies (antibodies produced against the body's own tissue), such as primary biliary cirrhosis (degeneration of liver tissue) and chronic active hepatitis (inflammation of the liver).

• Indirect Immunofluorescent Multiple Auto Antibody (FDA Code: DBL / 866.5660)

• Indirect Immunofluorescent Test, Antiparietal Antibody (FDA Code: DBJ / 866.5110)