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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• Insulin Test Strip

• Intrinsic Factor Blocking Antibody Radioassay (FDA Code: LIG / 862.1810) A vitamin B12test system is a device intended to measure vitamin B12in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of anemias of gastrointestinal malabsorption.

• Menopause Test strip (Urine)

• Methadone Test Strip

• Methamphetamine Test Strip

• Multi Analyte Processor

• Nuclear Pore Glycoprotein Gp210 Autoantibodies (FDA Code: NRI / 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).

• Outer-Membrane Proteins Antibodies (FDA Code: OKM / 866.5785) The Anti-Saccharomyces cerevisiae (S. cerevisiae ) antibody (ASCA) test system is an in vitro diagnostic device that consists of the reagents used to measure, by immunochemical techniques, antibodies toS. cerevisiae (baker's or brewer's yeast) in human serum or plasma. Detection ofS. cerevisiae antibodies may aid in the diagnosis of Crohn's disease.

• Ovulation Test Strip (Urine)

• Peracetic Acid Test Strips

• PeriScreen Test Strips

• pH Test Strips

• Phencyclidine Test Strip

• Pregnancy Test Strip (Urine/Serum)

• Product Development, Allergy Test Strips

• Prostate Specific Antigen Semi-Quantitative Rapid Test Strip

• Residual Chlorine Test Strips

• Residual Formaldehyde Test Strips

• Residual PeroxideTest Strips

• 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.

• Saccharomyces Cerevisiae (S.Cerevisiae) Antibodies (FDA Code: NBT / 866.5785)

• Sp100 Nuclear Body Protein Autoantibodies (FDA Code: NUM / 866.5090)

• Sugar Monitoring Test Strip

• 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).

• Thyroglobulin (FDA Code: DDC / 866.5870) A thyroid autoantibody immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the thyroid autoantibodies (antibodies produced against the body's own tissues). Measurement of thyroid autoantibodies may aid in the diagnosis of certain thyroid disorders, such as Hashimoto's disease (chronic lymphocytic thyroiditis), nontoxic goiter (enlargement of thyroid gland), Grave's disease (enlargement of the thyroid gland with protrusion of the eyeballs), and cancer of the thyroid.

• Thyroid Autoantibody Test System (FDA Code: JZO / 866.5870)

• Thyroid Thyroglobulin ELISA Kit

• Type 1) Lkm-1(Liver/Kidney Microsome Autoantibodies (FDA Code: NBS / 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).

• Uric Acid Test Strips

• Urinalysis Reagents & Test Strips

• Urinalysis Test Strips

• Urine Ketone Test Strip

• Water Quality Test Strips

• Water Quality Test Strips