# Citest Diagnostics Inc. (repackager or relabeler, VANCOUVER British Columbia, CA): 80 new FDA device listings, incl. diazo (colorimetric), nitrite (urinary, non-quant)

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Citest Diagnostics Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | VANCOUVER British Columbia, CA |
| New listings | 80 |
| Devices | Diazo (Colorimetric), Nitrite (Urinary, Non-Quant); Test, Urine Leukocyte; Thin Layer Chromatography, Morphine; Thin Layer Chromatography, Methamphetamine; Test, Methadone, Over The Counter; Enzyme Immunoassay, Methadone; Radioimmunoassay, Tricyclic Antidepressant Drugs; Enzyme Immunoassay, Amphetamine; Enzyme Immunoassay, Benzodiazepine; Enzyme Immunoassay, Opiates |
| Product codes | JMT, LJX, DNK, DJC, PTG, DJR, LFG, DKZ, JXM, DJG, NGI, NGG, NFW, QAW, LAF |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Clinical Chemistry, Hematology, Clinical Toxicology, Microbiology |
| Brand names | Citest Urinary Tract Infection Test; Citest Multi Drug Rapid Test Cup; Citest Multi Drug Test Panel; Citest Multi Drug Test Cup; Citest Multi Drug Rapid Test Panel; Citest Pregnancy Home Test; FSH Rapid Test Midstream; FSH Rapid Test Cassette |
| First new listing | 2026-10-21 |
| Latest new listing | 2026-10-22 |
| FDA registration number | 3023296261 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-11-04T21:52:36.524Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.