# UPS Supply Chain Solutions, Inc. (repackager or relabeler, Mira Loma, CA): 4 new FDA device listings, incl. enzyme linked immunoabsorbent assay, rubeola igg

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | UPS Supply Chain Solutions, Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Mira Loma, CA, US |
| New listings | 4 |
| Devices | Enzyme Linked Immunoabsorbent Assay, Rubeola Igg; Phenotypic Test Kit, Non-Susceptible/Elevated Mic Organisms, Cultured Isolates; Enzyme Linked Immunoabsorbent Assay, Mumps Virus; System, Mass Spectrometry, Maldi Tof, Microorganism Identification, Cultured Isolates |
| Product codes | LJB, PTJ, LJY, PEX |
| Device classes | Class I, Class II |
| Medical specialties | Microbiology |
| Brand names | VIDAS MEASLES IGG ASSAY; RAPIDEC CARBA NP; VIDAS Mumps (IgG) (MPG) Assay; VITEK MS MYCOB/NOCARDIA KIT; VITEK MS MOULD KIT |
| First new listing | 2026-07-29 |
| Latest new listing | 2026-07-29 |
| FDA registration number | 3009637528 |
| Registration expires | 2026-12-31 |

## Why this score
- 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: 2026-10-28T20:51:27.468Z.
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.