# Benev Company Inc (other, Mission Viejo, CA): 5 new FDA device listings, incl. electrosurgical, cutting & coagulation & accessories

**Score:** 75/100

| Field | Value |
|---|---|
| Establishment | Benev Company Inc |
| Owner / operator | BENEV Company Inc |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Mission Viejo, CA, US |
| New listings | 5 |
| Devices | Electrosurgical, Cutting & Coagulation & Accessories; Powered Microneedle Device; Powered Laser Surgical Instrument; Lamp, Infrared, Therapeutic Heating |
| Product codes | GEI, QAI, GEX, ILY |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery, Physical Medicine |
| Brand names | XTHERMA; SYLFIRM; CODE-X; SMARTLUX MINI |
| First new listing | 2026-10-20 |
| Latest new listing | 2026-10-20 |
| FDA registration number | 3003205477 |
| 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.
- Listed in the last 45 days.

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.