# iCRco Inc. (repackager or relabeler, Goleta, CA): 5 new FDA device listings, incl. camera, multi format, radiological

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | iCRco Inc. |
| Owner / operator | Icrco Inc. |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Goleta, CA, US |
| New listings | 5 |
| Devices | Camera, Multi Format, Radiological; System, X-Ray, Mobile; Solid State X-Ray Imager (Flat Panel/Digital Imager); System, X-Ray, Stationary |
| Product codes | LMC, IZL, MQB, KPR |
| Device classes | Class II |
| Medical specialties | Radiology |
| Brand names | iCRco CrystalM Imager; iCRco Crystal Imager; Fusion Mobile DR; AirDR-D; iXRS |
| First new listing | 2026-07-14 |
| Latest new listing | 2026-07-22 |
| FDA registration number | 3009717300 |
| 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.