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SAFElife™

Model TDOA-6135F · WONDFO USA CO., LTD. · DI 00816862028362

LCMEnzyme Immunoassay, Phencyclidine

NFTTest, Amphetamine, Over The Counter · Class II · 21 CFR 862.3100

NFVTest, Benzodiazepine, Over The Counter · Class II · 21 CFR 862.3170

NFWTest, Cannabinoid, Over The Counter · Class II · 21 CFR 862.3870

NFYTest, Cocaine And Cocaine Metabolites, Over The Counter · Class II · 21 CFR 862.3250

NGGTest, Methamphetamine, Over The Counter · Class II · 21 CFR 862.3610

NGLTest, Opiates, Over The Counter · Class II · 21 CFR 862.3650

PTGTest, Methadone, Over The Counter · Class II · 21 CFR 862.3620

PTHTest, Barbiturate, Over The Counter · Class II · 21 CFR 862.3150

UDILibrary device dossier · generated 2026-09-06 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

11222019-01: 0 reports for this device; peer average 1/device2019-02: 0 reports for this device; peer average 1/device2019-05: 0 reports for this device; peer average 1/device2019-06: 0 reports for this device; peer average 1/device2019-07: 0 reports for this device; peer average 1/device2019-10: 0 reports for this device; peer average 2/device2021-07: 0 reports for this device; peer average 1/device2022-06: 0 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 2/device2026-06: 0 reports for this device; peer average 2/device01020506071007060506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0101
2019-0201
2019-0501
2019-0601
2019-0701
2019-1002
2021-0701
2022-0601
2026-0502
2026-0602
This device (reports/month)Average device in LCM, NFT, NFV, NFW, NFY, NGG, NGL, PTG, PTH (reports/device/month)

Regulatory clearances

  • K252550 SESE 2025-11-18 (k number procode)

Predicate lineage

K252550 — cites (transitively): K182701 (d1), K122809 (d2)

Lineage extracted from public 510(k) summary text (heuristic).

Manufacturer compliance record — WONDFO USA CO., LTD.

  • VAI 2018-05-11 Wondfo USA Co Ltd · 4 citations
  • VAI 2018-05-11 Wondfo USA Co Ltd · 4 citations