510(k) Report

510(k) · Cleared

Cleared

Sure-Screen Amphetamine, Benzodiazepine, Cocaine, Methamphetamine/Mdma, Methadone, Opiates, Phencyclidine & Cannabinoids

K050394510(k) TraditionalCleared Oct 25, 2005251-day reviewClass II21 CFR 862.3100

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Medtox Diagnostics, Inc. · DKZ Enzyme Immunoassay, Amphetamine

Cleared on Oct 25, 2005 after a 251-day review. The FDA summary names no predicate by number. 3 later devices descend from it.

Decided
Oct 25, 2005
Review
251 days
Class
Class II
Product code
DKZ
Recalls
None
Predicates
0

3 later devices descend from it, 3 citing it directly.

Descendants, by year cleared 2013: 3 descendants cleared20052010201520202025
  1. This deviceK050394 Sure-Screen Amphetamine, Benzodiazepine, Cocaine…Medtox Diagnostics, Inc. · 2005
  2. Descendant · cites it directly · 0 of its ownK132630 Wondfo Oxazepam Urine Test (Bzo 200) and Wondfo Methamphetamine…Guangzhou Wondfo Biotech Co., Ltd. · 2013
  3. Descendant · cites it directly · 0 of its ownK131754 Wondfo Cocaine Urine Test (Coc 100), Wondfo Cannabinoids Urine Test…Guangzhou Wondfo Biotech Co., Ltd. · 2013
  4. Descendant · cites it directly · 0 of its ownK131232 Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test…Guangzhou Wondfo Biotech Co., Ltd. · 2013

Most influential descendants

Showing 3 of 3 · See all
  • K132630Wondfo Oxazepam Urine Test (Bzo 200) and Wondfo Methamphetamine Urine Test (Met 300)Guangzhou Wondfo Biotech Co., Ltd. · 2013 · cites it directly0descendants
  • K131754Wondfo Cocaine Urine Test (Coc 100), Wondfo Cannabinoids Urine Test (THC 40)Guangzhou Wondfo Biotech Co., Ltd. · 2013 · cites it directly0descendants
  • K131232Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100)Guangzhou Wondfo Biotech Co., Ltd. · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K050394Sure-Screen Amphetamine, Benzodiazepine, Cocaine, Methamphetamine/Mdma…Medtox Diagnostics, Inc.2005—
+1K132630Wondfo Oxazepam Urine Test (Bzo 200) and Wondfo Methamphetamine Urine Test…Guangzhou Wondfo Biotech Co., Ltd.2013—
+1K131754Wondfo Cocaine Urine Test (Coc 100), Wondfo Cannabinoids Urine Test (THC 40)Guangzhou Wondfo Biotech Co., Ltd.2013—
+1K131232Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100)Guangzhou Wondfo Biotech Co., Ltd.2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201330
FIG. 1 — Lineage of K050394, 2005–2013Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in DKZ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new DKZ device

  1. #1 K233019 AllTest Multi-Drug Rapid Test Cup; AllTest…score 14.6 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

The FDA summary names no predicate by number.

What descends from it? (3)

3 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K132630Wondfo Oxazepam Urine Test (Bzo 200) and Wondfo Methamphetamine Urine Test (Met 300)Guangzhou Wondfo Biotech Co., Ltd.20130
K131754Wondfo Cocaine Urine Test (Coc 100), Wondfo Cannabinoids Urine Test (THC 40)Guangzhou Wondfo Biotech Co., Ltd.20130
K131232Wondfo Methadone Urine Test (MTD 200), Wondofo Morphine Urine Test (Mop 100)Guangzhou Wondfo Biotech Co., Ltd.20130

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K132630 (Guangzhou Wondfo Biotech Co., Ltd., 2013) has gone furthest, with 0 descendants of its own.

How does its category compare?

All DKZ devices

DKZ Enzyme Immunoassay, Amphetamine: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DKZ

1in 2024

2008: 22009: 22010: 42011: 62012: 52013: 82014: 82015: 52016: 52018: 32019: 32020: 12023: 22024: 1
2007high 8 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DKZ

180in 2019

2010: 233 days median2011: 123 days median2012: 55 days median2013: 103 days median2014: 128 days median2015: 107 days median2016: 215 days median2018: 128 days median2019: 180 days median
2007high 233 (2010) · low 55 (2012)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · DKZ

1in 2017

2007: 12008: 32009: 52011: 42013: 12014: 32017: 1
2007high 5 (2009) · low 0 (2010)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DKZ

2in 2025

2008: 122009: 12010: 12011: 22013: 12014: 92015: 82016: 82021: 32022: 42023: 72024: 12025: 2
2007high 12 (2008) · low 0 (2007)2025

MAUDE reports naming product code DKZ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—10
20082—312
20092—51
2010423301
2011612342
201255500
2013810311
2014812839
2015510708
2016521508
20170—10
2018312800
2019318000
20201—00
20210—03
20220—04
20232—07
20241—01
20250—02
20260—0—

What is it indicated for?

The SURE-SCREEN Drugs of Abuse Test System uses immunochromatographic test strips for the rapid, qualitative detection of one or more of the following: Amphetamines, Benzodiazepines, Cocaine, Methamphetamine, Methadone, Opiates, Phencyciidine and THC (Cannabinoids) in human urine. It is intended for prescription point-of-care use including workplace settings, criminal justice or forensic settings, drug rehabilitation clinics, physician offices and…

Read the full statement (500 words)

The SURE-SCREEN Drugs of Abuse Test System uses immunochromatographic test strips for the rapid, qualitative detection of one or more of the following: Amphetamines, Benzodiazepines, Cocaine, Methamphetamine, Methadone, Opiates, Phencyciidine and THC (Cannabinoids) in human urine. It is intended for prescription point-of-care use including workplace settings, criminal justice or forensic settings, drug rehabilitation clinics, physician offices and laboratory settings. SURE-SCREEN is not for over-the-counter sale.

Operators that may use this device are defined as individuals with a minimum of a high school education with no formal laboratory training or experience. Individuals should also satisfy the following training and certification guidelines: (1)Training should be conducted by a qualified professional and include a demonstration of the SURE-SCREEN test system and (2) the use of quality assurance samples for monitoring and confirming the performance of the test system. Trainers should observe and confirm that the operator (3) uses proper technique when running a test sample and quality assurance samples, (4) has a basic understanding of test results, including a the potential for false positive and false negative results, (5) knows how to prepare a sample for shipment to the laboratory for confirmation testing, (6) has reviewed the information contained in the MEDTOX SURE-SCREEN Training and Certification Program (available at www.medtox.com and that the operator (7) minimally achieves a score of 80% on the written exam provided by MEDTOX.

Operators achieving a score of 80% will be provided with a certificate0of tfi'irkig ' participation. Quality assurance samples appropriate for trainng ar'-vadlblO,( - from MEDTOX Laboratories Inc. Additionally, MEDTOX Technical uppo&rwi!t provide access to assistance from individuals who are experienced the _~ interpretation of drug testing results.

Sure-Screen detects drug classes at the following cutoff concentrati ns:

(AMP) Amphetamines (d-Amphetamine) 300 ng/ L

(BZO) Benzodiazepines (Nordiazepam) 200 ng/mL

(COO) Cocaine (Benzoylecgonine) 100 ng/mL

(MAMP) Methamphetamine (d-Methamphetamine) 300 ng/mL

(MTD) Methadone (Methadone) 200 ng/mL

(OPI) Opiates (Morphine) 100 ng/mL

(POP) Phencyclidine (Phencyclidine) 925 ng/mL

9 40 ng/mL

(THC) Cannabinoids (11-nor-9-carboxy-A -THC)

Many of the cutoff concentrations for these tests are below those recommended by SAMHSA. Additionally, many of these tests are positive at levels significantly below the claimed cutoff concentration. The rate of false positive results with tests having sensitivities this low has not been studied. However, the rate of false positives generally increases as the cutoff concentration of the test is lowered. See the Precision/Sensitivity section for more information.

The SURE-SCREEN drugs of abuse test system provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GCIMS) or liquid chromatography/tandem mass spectrometry (LC/MSIMS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result.

It is the responsibility of those organizations required to follow Department of Transportation (DOT) or Substance Abuse Mental Health Services Administration (SAMHSA) Workplace Drug Testing Guidelines to determine that use of this product satisfies the criteria for workplace testing established under DOT and SAMHSA authority.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K050394: Sure-Screen Amphetamine, Benzodiazepine, Cocaine, Methamphetamine/Mdma, Methadone, Opiates, Phencyclidine & Cannabinoids.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050394

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026