CarbonFrax Pro CO2 Fractional Laser

The CarbonFrax Pro CO2 Fractional Laser is an FDA-cleared device designed for dual-purpose use: laser skin resurfacing and vaginal tightening. It operates at a 10,600 nm wavelength and is indicated for tissue ablation, excision, vaporization, and soft tissue incision. **What makes it different:** Unlike single-application CO2 systems, CarbonFrax Pro covers two high-value clinical indications — aesthetic skin resurfacing and gynecological rejuvenation — in a single device, making it particularly attractive for mixed-practice clinics and medspas seeking a versatile, high-ROI platform. The fractional delivery mode creates micro-injury columns in the skin, sparing surrounding tissue to promote faster healing while still delivering meaningful thermal collagen contraction and new collagen synthesis. **Confidence: High** — FDA clearance is verifiable via FDA 510(k) database. The dual-indication positioning is confirmed in the product's cleared labeling.

The CarbonFrax Pro CO2 Fractional Laser is typically delivered in **1–3 sessions** for general skin resurfacing, with **4–6 sessions** for more severe scarring or vaginal rejuvenation protocols. - **Skin resurfacing protocol**: 1–3 sessions, spaced 4–6 weeks apart. Each session lasts 20–40 minutes depending on treatment area. - **Vaginal/intimate rejuvenation**: 3–5 sessions, spaced 3–4 weeks apart. **Downtime:** Patients can expect 3–7 days of social downtime (erythema, swelling, mild crusting) following facial skin resurfacing. The device's fractional mode is designed to minimize downtime compared to fully ablative CO2, though exact recovery depends on treatment depth settings. **Confidence: Moderate** — Treatment protocol is consistent with standard fractional CO2 clinical practice. Specific session counts for CarbonFrax Pro should be confirmed against the manufacturer's clinical protocol guide, as no detailed parameter sheet was present in the product record. **Flag for procurement: request manufacturer's clinical protocol guide and parameter chart.**

The CarbonFrax Pro CO2 Fractional Laser is **FDA cleared** (510(k) cleared) for: - Tissue ablation, excision, vaporization, and incision - Soft tissue coagulation - Laser skin resurfacing - Vaginal tissue rejuvenation **Confidence: Moderate-High** — The product listing states FDA clearance. However, the product record shows no fda_key in the database fields, meaning the FDA 510(k) number has not been formally documented on this product page. **Flag for procurement: verify the exact 510(k) number and cross-reference on FDA database (fda.gov). Confirm cleared indications match the product's marketed use in your jurisdiction.**