# Labsource, Inc (specification developer, Northlake, IL): 7 new FDA device listings, incl. polymer patient examination glove

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Labsource, Inc |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Northlake, IL, US |
| New listings | 7 |
| Devices | Polymer Patient Examination Glove; Fentanyl And Other Opioid Protection Glove; Medical Gloves With Chemotherapy Labeling Claims - Test For Use With Chemotherapy Drugs; Medical Glove, Specialty |
| Product codes | LZA, QDO, OPJ, LZC |
| Device classes | Class I |
| Medical specialties | General Hospital |
| First new listing | 2026-10-13 |
| Latest new listing | 2026-10-13 |
| FDA registration number | 3012429634 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Several new listings at once.
- U.S. establishment.
- 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: 2026-10-28T20:51:27.468Z.
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.