# Glownar Aesthetics. LLC (specification developer, Davie, FL): 10 new FDA device listings, incl. light based over the counter wrinkle reduction

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | Glownar Aesthetics. LLC |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Davie, FL, US |
| New listings | 10 |
| Devices | Light Based Over The Counter Wrinkle Reduction; Over-The-Counter Powered Light Based Laser For Acne; Powered Laser Surgical Instrument; Low Power Electrosurgical Devices For Skin Lesion Destruction; Powered Microneedle Device; Electrosurgical, Cutting & Coagulation & Accessories; Brush, Dermabrasion, Powered; Powered Light Based Non-Laser Surgical Instrument With Thermal Effect |
| Product codes | OHS, OLP, GEX, QVJ, QAI, GEI, GFE, ONF |
| Device classes | Class I, Class II |
| Medical specialties | General, Plastic Surgery |
| Brand names | Velour LED Face Mask; Verso Optix Pro 1 Diode Laser Hair Removal with Interchangeable Spot Size; Torno Diode Laser Hair Removal with 4 wavelengths; Veloce 808 Diode 3 Laser Hair Removal; The Veloce Diode 3 Laser Hair Removal; Verso Optix Pro 2 Diode Laser Hair Removal; Plasmoderm X Fractional & Cold Plasma; Velvet Microneedling Pen |
| First new listing | 2026-05-13 |
| Latest new listing | 2026-09-24 |
| FDA registration number | 3022327202 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- 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.