510(k) Report

510(k) · Cleared

Cleared

SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel Dx

K260065510(k) TraditionalCleared Apr 28, 2026109-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

Guangzhou Wondfo Biotech Co., Ltd. · NFT Test, Amphetamine, Over The Counter

Cleared on Apr 28, 2026 as substantially equivalent to K202567 (Guangzhou Wondfo Biotech Co., Ltd., 2020) after a 109-day review. Its family tree reaches back 8 generations to 1995.

Decided
Apr 28, 2026
Review
109 days
Class
Class II
Product code
NFT
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K945610 (1995). 29 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 8 generations backK945610 Abusign (TM) Amp, Doa-Amp, Accusign (TM) Amp-Doa-Amp, Biosign (TM)…Princeton BioMeditech Corp. · 1995
  2. 7 generations backK011673 Acon Amp One Step Amphetamine Test Strip, Acon Amp One Step…ACON Laboratories, Inc. · 2001
  3. 6 generations backK020313 Acon One Step Multi-Drug Multi-Line Screen Test Card; Acon One Step…Acon Laboratories Co. · 2002
  4. 5 generations backK031759 Acon Spectrum Multi-Drug Multi-Line Drug Screen Test Card and Acon…ACON Laboratories, Inc. · 2003 · Recalled
  5. 4 generations backK061718 Innovacon Spectrum II Test CardInnovacon, Inc. · 2006 · Recalled
  6. 3 generations backK122809 Advin Multi-Drug Screen Test Cassette, Dip Card and CupAdvin Biotech · 2013
  7. 2 generations backK182701 Wondfo T-Cup Multi-Drug Urine Test CupGuangzhou Wondfo Biotech Co., Ltd. · 2018 · Recalled
  8. 1 generation backK202567 Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug…Guangzhou Wondfo Biotech Co., Ltd. · 2020
  9. This deviceK260065 SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip…Guangzhou Wondfo Biotech Co., Ltd. · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K945610Abusign (TM) Amp, Doa-Amp, Accusign (TM) Amp-Doa-Amp, Biosign (TM) Amp, Doa-AmpPrinceton BioMeditech Corp.1995—
−7K011673Acon Amp One Step Amphetamine Test Strip, Acon Amp One Step Amphetamine Test…ACON Laboratories, Inc.2001—
−6K020313Acon One Step Multi-Drug Multi-Line Screen Test Card; Acon One Step Multi-Drug…Acon Laboratories Co.2002—
−5K031759Acon Spectrum Multi-Drug Multi-Line Drug Screen Test Card and Acon Spectrum…ACON Laboratories, Inc.20031
−4K061718Innovacon Spectrum II Test CardInnovacon, Inc.20066
−3K122809Advin Multi-Drug Screen Test Cassette, Dip Card and CupAdvin Biotech2013—
−2K182701Wondfo T-Cup Multi-Drug Urine Test CupGuangzhou Wondfo Biotech Co., Ltd.20181
−1K202567Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug Urine Test…Guangzhou Wondfo Biotech Co., Ltd.2020—
0 (this device)K260065SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine…Guangzhou Wondfo Biotech Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199620
199810
199910
200010
200170
200220
200320
200430
200510
200610
FIG. 1 — Lineage of K260065, 1995–2026Source: 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 NFT? 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 NFT device

  1. #1 K244043 AllTest Multi-Drug Rapid Test Cup ; AllTest…score 20.3 · 9 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? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K202567Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug Urine Test Panel Rx
Summary page 7
…System 6. Predicate Device Product name: Wondfo T-Dip Multi-Drug Urine Test Panel, Wondfo T-Dip Multi-Drug Urine Test Panel Rx 510(k) Number: K202567 7. Intended Use SAFElife™ T-Dip Multi-Drug Urine Test Panel is a competitive binding, lateral flow immunochromatogr…
Guangzhou Wondfo Biotech Co., Ltd.2020—

Also cleared against K202567: 2 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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?

  • The line of descent spans 31 years and passes through 6 companies; a new generation was cleared every 5.5 years on median.
  • 3 of the 29 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K202567.

How does its category compare?

All NFT devices

NFT Test, Amphetamine, Over The Counter: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · NFT

8in 2025

2017: 12018: 62019: 12020: 22021: 12022: 32023: 12024: 42025: 82026 (partial year): 5
2007high 8 (2025) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NFT

37in 2025

2018: 56 days median2022: 63 days median2024: 31 days median2025: 37 days median2026 (partial year): 35 days median
2007high 63 (2022) · low 31 (2024)2026

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

Recalls per year · NFT

No recall names NFT since 2007.

Adverse event reports per year · NFT

No MAUDE report names NFT since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20171—00
201865600
20191—00
20202—00
20211—00
202236300
20231—00
202443100
202583700
20265350—

What is it indicated for?

SAFElife™ T-Dip Multi-Drug Urine Test Panel is a competitive binding, lateral flow immunochromatographic assay for qualitative and simultaneous detection of 6-Monoacetylmorphine, Amphetamine, Buprenorphine, Secobarbital, Oxazepam, Cocaine, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), Fentanyl, Methamphetamine, Methylenedioxymethamphetamine, Morphine, Opiates, Methadone, Norfentanyl, Oxycodone, Phencyclidine, Propoxyphene, Nortriptyline…

Read the full statement (605 words)

SAFElife™ T-Dip Multi-Drug Urine Test Panel is a competitive binding, lateral flow immunochromatographic assay for qualitative and simultaneous detection of 6-Monoacetylmorphine, Amphetamine, Buprenorphine, Secobarbital, Oxazepam, Cocaine, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), Fentanyl, Methamphetamine, Methylenedioxymethamphetamine, Morphine, Opiates, Methadone, Norfentanyl, Oxycodone, Phencyclidine, Propoxyphene, Nortriptyline, Cannabinoids and Tramadol in human urine at the cutoff concentrations of:

Drug (Identifier) Cutoff Level

6-Monoacetylmorphine(6-MAM) 10 ng/mL

Amphetamine (AMP) 1000 ng/mL or 500 ng/mL

Buprenorphine (BUP) 10 ng/mL

Secobarbital (BAR) 300 ng/mL

Oxazepam (BZO) 300 ng/mL

Cocaine (COC) 300 ng/mL or 150 ng/mL

2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) 300 ng/mL

Fentanyl (FTY) 1 ng/mL

Methamphetamine (MET/mAMP) 1000 ng/mL or 500 ng/mL

Methylenedioxymethamphetamine (MDMA) 500 ng/mL

Morphine (MOP)) 300 ng/mL

Opiates (OPI) 2000 ng/mL

Methadone (MTD) 300 ng/mL

Norfentanyl (NFTY) 5 ng/mL

Oxycodone (OXY) 100 ng/mL

Phencyclidine (PCP) 25 ng/mL

Propoxyphene (PPX) 300 ng/mL

Nortriptyline (TCA) 1000 ng/mL

Cannabinoids (THC) 50 ng/mL or 20 ng/mL

Tramadol (TRA) 100 ng/mL

SAFElife™ T-Dip Multi-Drug Urine Test Panel offers any combinations from 1 to 15 drugs of abuse tests listed above but only one cutoff concentration under same drug condition will be included per device. It is for in vitro diagnostic use.

The tests may yield positive results for the prescription drugs Buprenorphine, Fentanyl, Nortriptyline, Oxazepam, Secobarbital, Oxycodone and Tramadol when taken at or above prescribed doses. It is not intended to distinguish between prescription use or abuse of these drugs. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly in evaluating a preliminary positive result.

The tests provide only preliminary results. To obtain a confirmed analytical result, a more specific alternate chemical method must be used. Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectrometry (LC/MS) is the recommended confirmatory method.

SAFElife™ T-Dip Multi-Drug Urine Test Panel Dx is a competitive binding, lateral flow immunochromatographic assay for qualitative and simultaneous detection of 6-Monoacetylmorphine, Amphetamine, Secobarbital, Buprenorphine, Oxazepam, Cocaine, 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP), Fentanyl, Methylenedioxymethamphetamine, Methamphetamine, Morphine, Opiates, Methadone, Norfentanyl, Oxycodone, Phencyclidine, Propoxyphene, Nortriptyline, Cannabinoids and Tramadol in human urine with below cutoff concentrations:

Drug (Identifier) Calibrator Cut-off Level

6-Monoacetylmorphine (6-MAM) 6-Monoacetylmorphine 10 ng/mL

Amphetamine (AMP500) d-Amphetamine 500 ng/mL

Amphetamine (AMP1000) d-Amphetamine 1000 ng/mL

Secobarbital (BAR) Secobarbital 300 ng/mL

Buprenorphine (BUP) Buprenorphine 10 ng/mL

Oxazepam (BZO) Oxazepam 300 ng/mL

Cocaine (COC150) Benzoylecgonine 150 ng/mL

Cocaine (COC300) Benzoylecgonine 300 ng/mL

2-ethylidene-1,5-dimethyl-3, 3-diphenylpyrrolidine (EDDP) 2-ethylidene-1,5-dimethyl-3, 3-diphenyl-pyrrolidine 300 ng/mL

Fentanyl (FTY) Fentanyl 1 ng/mL

Methylenedioxymethamphetamine (MDMA) 3,4-Methylenedioxymethamphetamine 500 ng/mL

Methamphetamine (MET500/mAMP500) D(+)-Methamphetamine 500 ng/mL

Methamphetamine (MET1000/mAMP1000) D(+)-Methamphetamine 1000 ng/mL

Morphine (MOP300) Morphine 300 ng/mL

Opiates (OPI2000) Morphine 2000 ng/mL

Methadone (MTD) Methadone 300 ng/mL

Norfentanyl (NFTY) Norfentanyl 5 ng/mL

Oxycodone (OXY) Oxycodone 100 ng/mL

Phencyclidine (PCP) Phencyclidine 25 ng/mL

Propoxyphene (PPX) d-Propoxyphene 300 ng/mL

Nortriptyline (TCA) Nortriptyline 1000 ng/mL

Cannabinoids (THC20) 11-nor- 9-THC-9-COOH 20 ng/mL

Cannabinoids (THC50) 11-nor- 9-THC-9-COOH 50 ng/mL

Tramadol (TRA) Tramadol 100 ng/mL

SAFElife™ T-Dip Multi-Drug Urine Test Panel Dx offers any combinations from 1 to 15 drugs of abuse tests listed above with or without on-board adulteration/specimen validity test (SVT) but only one cutoff concentration under same drug condition will be included per device. It is for in vitro diagnostic use.

The tests may yield positive results for the prescription drugs Buprenorphine, Fentanyl, Nortriptyline, Oxazepam, Secobarbital, Oxycodone and Tramadol when taken at or above prescribed doses. It is not intended to distinguish between prescription use or abuse of these drugs. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly in evaluating a preliminary positive result.

The tests provide only preliminary results. To obtain a confirmed analytical result, a more specific alternate chemical method must be used. Gas Chromatography/Mass Spectrometry (GC/MS) or Liquid Chromatography/Mass Spectrometry (LC/MS) is the recommended confirmatory method.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K260065: SAFElife T-Dip Multi-Drug Urine Test Panel; SAFElife T-Dip Multi-Drug Urine Test Panel Dx.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K260065

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026