# Live Tulani, LLC (repackager or relabeler, Farmington, UT): 6 new FDA device listings, incl. system, test, blood glucose, over the counter

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Live Tulani, LLC |
| Role | Repackager or relabeler |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device |
| Location | Farmington, UT, US |
| New listings | 6 |
| Devices | System, Test, Blood Glucose, Over The Counter; Multiple Use Blood Lancet For Single Patient Use Only; Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature; Single (Specified) Analyte Controls (Assayed And Unassayed); Glucose Oxidase, Glucose |
| Product codes | NBW, QRL, QRK, JJX, CGA |
| Device classes | Class I, Class II |
| Medical specialties | Clinical Chemistry, General, Plastic Surgery |
| Brand names | Tulani Air Strips; Tulani Lancets; Tulani Air |
| First new listing | 2026-05-29 |
| Latest new listing | 2026-05-29 |
| FDA registration number | 3045951983 |
| 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: 2026-11-04T21:52:36.524Z.
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.