Medicaid Provider Spending

$1.09 trillion in Medicaid claims data, 2018–2024 · 617K+ providers

ACE BIOMEDICAL LABS, LLC

NPI: 1750839262 · JACKSONVILLE, FL 32216 · Clinical Medical Laboratory · NPI assigned 09/13/2016

$222K
Total Medicaid Paid
19,744
Total Claims
13,258
Beneficiaries
21
Codes Billed
2018-06
First Month
2024-12
Last Month

Provider Details

Authorized OfficialSHARMA, MADHUKAR (OWNER)
NPI Enumeration Date09/13/2016

Related Entities

Other providers sharing the same authorized official: SHARMA, MADHUKAR

ProviderCityStateTotal Paid
SOUTHERN PLAINS MEDICAL CENTER OF GARVIN COUNTY LLC PAULS VALLEY OK $1.29M
OM DIAGNOSTIC LABORATORIES INC. NORWOOD MA $1.05M
FORENSIC STAT LABORATORY INC CORAL SPRINGS FL $63K

Monthly Spending Trend

Yearly Breakdown

YearClaimsTotal Paid
2018 755 $0.00
2019 1,100 $35.17
2020 1,674 $20K
2021 7,527 $97K
2022 4,859 $79K
2023 2,885 $21K
2024 944 $5K

Billing Codes

CodeDescriptionClaimsBeneficiariesTotal Paid
U0003 Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, making use of high throughput technologies as described by cms-2020-01-r 4,780 2,826 $160K
U0005 Infectious agent detection by nucleic acid (dna or rna); severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), amplified probe technique, cdc or non-cdc, making use of high throughput technologies, completed within 2 calendar days from date of specimen collection (list separately in addition to either hcpcs code u0003 or u0004) as described by cms-2020-01-r2 4,210 2,497 $18K
80307 Drug test(s), presumptive, any number of drug classes; immunoassay 2,644 2,063 $17K
G0481 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 8-14 drug class(es), including metabolite(s) if performed 2,004 1,578 $11K
G2023 Specimen collection for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]), any specimen source 3,463 2,115 $10K
87631 54 26 $4K
K1034 Provision of covid-19 test, nonprescription self-administered and self-collected use, fda approved, authorized or cleared, one test count 1,147 1,105 $640.32
87498 53 25 $192.06
87502 Infectious agent detection by nucleic acid, influenza virus, for multiple types or subtypes, includes all targets 44 18 $105.38
87634 44 18 $46.97
87798 Infectious agent detection by nucleic acid; not otherwise specified, amplified probe, each organism 45 19 $42.28
87503 43 18 $31.68
85025 Blood count; complete (CBC), automated, and automated differential WBC count 176 115 $14.30
80053 Comprehensive metabolic panel 49 26 $0.00
G2024 Specimen collection for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) (coronavirus disease [covid-19]) from an individual in a snf or by a laboratory on behalf of a hha, any specimen source 94 72 $0.00
36415 Collection of venous blood by venipuncture 66 32 $0.00
P9603 Travel allowance one way in connection with medically necessary laboratory specimen collection drawn from home bound or nursing home bound patient; prorated miles actually travelled 58 27 $0.00
G0480 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 1-7 drug class(es), including metabolite(s) if performed 50 33 $0.00
86140 21 12 $0.00
G0483 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 22 or more drug class(es), including metabolite(s) if performed 184 182 $0.00
G0482 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 15-21 drug class(es), including metabolite(s) if performed 515 451 $0.00