Eiranthia Pro Fractional RF Microneedling System

The Eiranthia Pro Fractional RF Microneedling System is a professional-grade 3-in-1 system combining 1 MHz fractional RF microneedling, vacuum-assisted RF, and cold hammer cooling — built around a large 13.3" LCD touchscreen interface with adjustable needle depths of 0.1–3.0 mm. **What makes it different:** The triple-modality approach (RF microneedling + vacuum-assisted RF + cold hammer) is more comprehensive than most RF microneedling platforms. The vacuum-assisted RF function provides an additional non-needle skin tightening option, while the cold hammer enables post-treatment soothing. The 50W RF power and 0.1–3.0 mm depth range indicate a device designed for precision — particularly for finer work around the eyes and lips where shallow depth is critical. **Confidence: Moderate** — Multi-modality design confirmed in product data. No FDA clearance documented in product record.

The Eiranthia Pro's triple-modality design supports flexible treatment protocols: **RF Microneedling module:** - Skin rejuvenation / tightening: 3–4 sessions, 4–6 week intervals - Acne scars / stretch marks: 4–6 sessions, 4–6 week intervals - Needle depth: 0.1–3.0 mm (precision range for fine facial areas) **Vacuum-Assisted RF module:** - Non-needle skin tightening: 4–6 sessions, 2–4 week intervals - Suitable for patients who want RF benefits without needle penetration **Downtime:** RF microneedling with Eiranthia Pro: **1–3 days of mild erythema**. Vacuum-assisted RF: **minimal to no downtime** (0–1 day). Cold hammer post-treatment: helps reduce post-procedure redness, enabling faster return to normal activities. **Confidence: Moderate** — Protocol consistent with category. **Flag for procurement: request manufacturer parameter guides, particularly for the vacuum-assisted RF function which is less standardized. Verify FDA status for all three modules independently.**

The Eiranthia Pro Fractional RF Microneedling System FDA status **cannot be confirmed from current product data** — the fda_key field is empty and no FDA clearance claim is present in the product database. **Confidence: Low** — No FDA clearance is documented. **Flag for procurement: confirm FDA clearance status for all three modules (RF microneedling, vacuum-assisted RF, cold hammer) independently. Vacuum-assisted RF is a less standardized modality — verify its specific clearance indication. Do not market as FDA cleared without documented evidence.**