# Q1 ,LLC (repackager or relabeler, Orlando, FL): 2 new FDA device listings, incl. needle, catheter

**Score:** 35/100

| Field | Value |
|---|---|
| Establishment | Q1 ,LLC |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Orlando, FL, US |
| New listings | 2 |
| Devices | Needle, Catheter; Syringe, Irrigating (Non Dental) |
| Product codes | GCB, KYZ |
| Device classes | Class I |
| Medical specialties | General, Plastic Surgery, General Hospital |
| First new listing | 2026-06-25 |
| Latest new listing | 2026-06-25 |
| FDA registration number | 3016676855 |
| Registration expires | 2026-12-31 |

## Why this score
- 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.