# Metropolis International, LLC (repackager or relabeler, Long Island City, NY): 2 new FDA device listings, incl. system, nuclear magnetic resonance imaging

**Score:** 50/100

| Field | Value |
|---|---|
| Establishment | Metropolis International, LLC |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Long Island City, NY, US |
| New listings | 2 |
| Devices | System, Nuclear Magnetic Resonance Imaging; System, X-Ray, Tomography, Computed |
| Product codes | LNH, JAK |
| Device classes | Class II |
| Medical specialties | Radiology |
| Brand names | Metropolis International; Esaote G-Scan Brio; GE Performix Tube |
| First new listing | 2026-09-10 |
| Latest new listing | 2026-09-10 |
| FDA registration number | 3005877899 |
| Registration expires | 2026-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- 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.