FDA device listing

Healgen Accurate Home Urine Drug Test Dip Card,Healgen Accurate Urine Drug Screen Dip Card;

FDA device listing 1856984927 · Zhejiang Orient Gene Biotech Co., Ltd

Key facts

Proprietary names Healgen Accurate Home Urine Drug Test Dip Card,Healgen Accurate Urine Drug Screen Dip Card;
Owner/operator Zhejiang Orient Gene Biotech Co., Ltd
Owner/operator number 10033347
Product codes NFT, NFV, NFW, NFY, NGG, NGL, NGM, PTG, PTH, QAW, QBF
Device names NFT - Test, Amphetamine, Over The Counter, NFV - Test, Benzodiazepine, Over The Counter, NFW - Test, Cannabinoid, Over The Counter, NFY - Test, Cocaine And Cocaine Metabolites, Over The Counter, NGG - Test, Methamphetamine, Over The Counter, NGL - Test, Opiates, Over The Counter, NGM - Test, Phencyclidine (Pcp), Over The Counter, PTG - Test, Methadone, Over The Counter, PTH - Test, Barbiturate, Over The Counter, QAW - Test, Tricyclic Antidepressants, Over The Counter, QBF - Test, Propoxyphene, Over The Counter
Device class Class II, Unclassified
Classification regulations (21 CFR) 862.3100, 862.3150, 862.3170, 862.3250, 862.3610, 862.3620, 862.3650, 862.3700, 862.3870, 862.3910, ORCA1.NGM
Review panels Clinical Toxicology
Registered establishments ZHEJIANG ORIENT GENE BIOTECH
Establishment registrations 3008517993
FEI numbers 3008517993
Establishment operations Contract Manufacturer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • None listed Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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