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HCPCS S3620: Newborn Metabolic Screening Panel, Kit and Tests
HCPCS Level II code S3620 represents a packaged newborn metabolic screening panel that covers the test kit, postage, and the state-specified laboratory assays used to identify inborn errors of metabolism and other congenital conditions in neonates. Newborn screening is a routine public-health service performed shortly after birth and is vital for early detection and timely intervention to prevent serious morbidity.
Key payers in this analysis include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find a concise clinical and billing overview of the code, typical sites of service, common modifiers associated with laboratory and ancillary services, and a summary of how this HCPCS Level II code is used in newborn screening workflows. The publication outlines benchmark topics such as coverage inclusion, packaging of test kits and postage within a single code, and common billing considerations for inpatient newborn nursery and outpatient newborn screening programs.
The content provides national context for payers and administrators, clarifies the service type and expected clinical use, and flags areas where payers often define coverage policy or billing requirements. Data not available in the input: specific payer policy details, reimbursement rates, associated taxonomies, ICD-10 diagnoses, and related codes.
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Billing Code Overview
HCPCS Level II code S3620 describes a newborn metabolic screening panel that includes the test kit, postage, and the laboratory tests specified by the state for inclusion in the panel. Examples of tests commonly included in this panel are galactose, hemoglobin electrophoresis, 17-hydroxyprogesterone (17-OHP), phenylalanine (PKU), and total thyroxine (T4).
Service Type: Newborn screening laboratory services, packaged kit and testing
Typical Site of Service: Hospital newborn nursery, birthing center, or public health laboratory setting