# Mlife Diagnostics LLC (contract manufacturer, Marshall, TX): 11 new FDA device listings, incl. test, cannabinoid, over the counter

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Mlife Diagnostics LLC |
| Owner / operator | mLife Diagnostics LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Marshall, TX, US |
| New listings | 11 |
| Devices | Test, Cannabinoid, Over The Counter; Test, Methamphetamine, Over The Counter; Test, Amphetamine, Over The Counter; Test, Tricyclic Antidepressants, Over The Counter; Test, Phencyclidine (Pcp), Over The Counter; Test, Methadone, Over The Counter; Test, Propoxyphene, Over The Counter; Test, Cocaine And Cocaine Metabolites, Over The Counter; Test, Opiates, Over The Counter; Test, Benzodiazepine, Over The Counter |
| Product codes | NFW, NGG, NFT, QAW, NGM, PTG, QBF, NFY, NGL, NFV, PTH |
| Device classes | Class II, Unclassified |
| Medical specialties | Clinical Toxicology |
| Brand names | mLife Rapid Drug Test |
| First new listing | 2026-07-17 |
| Latest new listing | 2026-07-17 |
| FDA registration number | 3017060097 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- U.S. establishment.

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.