# Laser Marketing Group, LLC (repackager or relabeler, Lehi, UT): 5 new FDA device listings, incl. electrosurgical, cutting & coagulation & accessories

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Laser Marketing Group, LLC |
| Role | Repackager or relabeler |
| Establishment types | Repack or Relabel Medical Device |
| Location | Lehi, UT, US |
| New listings | 5 |
| Devices | Electrosurgical, Cutting & Coagulation & Accessories; Powered Laser Surgical Instrument |
| Product codes | GEI, GEX |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | XERF; Sciton MJoule; PICOSURE PRO; LaseMD Ultra; LightPod Neo Elite |
| First new listing | 2026-05-19 |
| Latest new listing | 2026-08-07 |
| FDA registration number | 3009736547 |
| 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.