Clarity Diagnostics, LLC

FDA Device Registration & Listing · Deerfield Bch, FL, US · Registration 3004043187

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004043187
FEI Number
3004043187
Entity Name
Clarity Diagnostics, LLC
City/State/Country
Deerfield Bch, FL, US
Establishment Address
1701 Green Rd Ste A, Deerfield Bch, FL 33064, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
33487 (Owner Number: 9057600)
Owner / Operator Contact Address
1060 Holland Dr STE A, --, Boca Raton, FL 33487, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Clarity Mononucleosis Test Clarity Urine Pregnancy Tests Clarity Glucose Meter Clarity Urocheck Urine Strips Clarity Rapid Strep A test Clarity Urocheck Urine Strips Clarity Urine HCG Pregnancy Tests Clarity Rapid Strep A test

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KTN System, Test, Infectious Mononucleosis Immunology Class 2 866.5640 2008-02-04
JHI Visual, Pregnancy Hcg, Prescription Use Clinical Chemistry Class 2 862.1155 2008-02-12
CGA Glucose Oxidase, Glucose Clinical Chemistry Class 2 862.1345 2008-02-04
NBW System, Test, Blood Glucose, Over The Counter Clinical Chemistry Class 2 862.1345 2008-02-04
LJX Test, Urine Leukocyte Hematology Class 1 864.7675 2008-02-14
JMT Diazo (Colorimetric), Nitrite (Urinary, Non-Quant) Clinical Chemistry Class 1 862.1510 2008-02-14
JIN Nitroprusside, Ketones (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1435 2008-02-14
JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1645 2008-02-14
JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative) Clinical Chemistry Class 2 862.1340 2008-02-14
CEN Dye-Indicator, Ph (Urinary, Non-Quantitative) Clinical Chemistry Class 1 862.1550 2008-02-14
JRE Refractometer For Clinical Use Clinical Chemistry Class 1 862.2800 2008-02-14
JIO Blood, Occult, Colorimetric, In Urine Hematology Class 2 864.6550 2008-02-14
JMA Acid, Ascorbic, 2,4-Dinitrophenylhydrazine (Spectrophotometric) Clinical Chemistry Class 1 862.1095 2008-02-14
CDM Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1785 2008-02-14
JJB Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1115 2008-02-14
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2003-07-24
CEN Dye-Indicator, Ph (Urinary, Non-Quantitative) Clinical Chemistry Class 1 862.1550 2008-02-14
JIO Blood, Occult, Colorimetric, In Urine Hematology Class 2 864.6550 2008-02-14
LJX Test, Urine Leukocyte Hematology Class 1 864.7675 2008-02-14
JMT Diazo (Colorimetric), Nitrite (Urinary, Non-Quant) Clinical Chemistry Class 1 862.1510 2008-02-14
JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative) Clinical Chemistry Class 2 862.1340 2008-02-14
JJB Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1115 2008-02-14
JRE Refractometer For Clinical Use Clinical Chemistry Class 1 862.2800 2008-02-14
CDM Diazonium Colorimetry, Urobilinogen (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1785 2008-02-14
JIN Nitroprusside, Ketones (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1435 2008-02-14
JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.) Clinical Chemistry Class 1 862.1645 2008-02-14
JHI Visual, Pregnancy Hcg, Prescription Use Clinical Chemistry Class 2 862.1155 2006-01-04
GTY Antigens, All Groups, Streptococcus Spp. Microbiology Class 1 866.3740 2006-01-04

Official Correspondent

Richard Simpson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

33487
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K964536 Teco Diagnostics ONE-STEP DIPSTICK PREGNANCY TEST 1997-02-11
K904016 Bhc Biotech , Ltd. MAXI TEST 1990-10-15
K870259 Leeco Diagnostics, Inc. VIS-CUBE HCG (EIA) LYOPHILIZED JPL-044 1987-03-10
K820822 Hybritech, Inc. TANDEM HCG KIT 1982-04-29
K811074 Reagents Applications, Inc. GLUCOSE REAGENT-ENZYMATIC-COLOR 500 1981-04-29

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0006-05 Abbott Health Products, Inc. 2
AxSYM Total B-hCG Reagent, Product list number: 7A59-22 and 7A59-21
Z-0378-06 Instrumentation Laboratory Co. 2
GEM PREMIER 3000
Z-2165-2011 Instrumentation Laboratory Co. 2
Instrumentation Laboratory GEM Premier 4000 PN 00025000000 The GEM Premier 4000 is a portable critical care system for use by health care professionals to rapidly analyze whole blood samples at the point of health care delivery in a clinical setting and in a central laboratory. The instrument provides quantitative measurements of pH, pC02, p02, sodium, potassium, chloride, ionized calcium, glucose, lactate, hematocrit, total bilirubin and CO-OXimetry (tHb, 02Hb, COHb, MetHb, HHb) parameters. Total bilirubin can also be quantitated from heparinized plasma samples when analyzed in the tBili/CO-Ox mode. These parameters, along with derived parameters, aid in the diagnosis of a patient's acidlbase status, electrolyte and metabolite balance and oxygen delivery capacity. Total bilirubin measurements are used in the diagnosis and management of biliary tract obstructions, liver disease and various hemolytic diseases and disorders involving the metabolism of bilirubin. In neonates, the level of total bilirubin is used to aid in assessing the risk of kernicterus
Z-0004-2009 Lifescan Inc 2
One Touch Ultra Test Strips, part number 020-994-02, manufactured by LifeScan Inc, Milpitas, CA, 25 count. Intended to be used for quantitative measurement of glucose in fresh capillary whole blood. Intended for use outside the body (in vitro diagnostic use) by people with diabetes at home and healthcare professionals in a clinical setting as an aid to monitor the effectiveness of diabetes control. Intended for use on the finger, arm, or palm.
Z-0042-06 Abbott Laboratories Medisense Products 2
FreeStyle FLASH Blood Glucose Monitoring System; Recalling Firm/Manufacturer: Abbott Diabetes Care, Inc., 1360 South Loop Road, Alameda, CA 94502

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004043187. Last updated year: 2026. Please use registration number 3004043187 when referencing this establishment in official correspondence.
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