InMode Morpheus8 Prime
RF Microneedling · Small-tip RF microneedling for periorbital
InMode Morpheus8 Prime pricing is not published by the manufacturer, and we have not yet verified a US market range. InMode Morpheus8 Prime holds FDA 510(k) clearance for its marketed indication. Figures are market estimates verified August 6, 2026.
What it's actually cleared for: Cleared for dermatological and general surgical procedures for electrocoagulation and hemostasis; family clearance shared across the Morpheus8 platform.
Last verified: August 6, 2026 · How we verify
New: —|Used: —market estimate, no email required
| Manufacturer | InMode |
|---|---|
| Company | Owner: Publicly traded (NASDAQ: INMD; no single controlling owner) (public company, since 2019) · Distribution: direct |
| Category | RF Microneedling, Tightening & HIFU |
| Technology | Small-tip RF microneedling for periorbital |
| FDA status | FDA Cleared |
| New price range | Not published |
| Used price range | Not published |
| Consumables | Not published |
| Launch year | 2023 |
| Last verified | August 6, 2026 |
Overview
Eye-area-focused Morpheus8 variant
FDA & regulatory status
What it's actually cleared for:
Cleared for dermatological and general surgical procedures for electrocoagulation and hemostasis; family clearance shared across the Morpheus8 platform.
510(k) numbers
K192695; K240017
Regulatory data is compiled from public FDA 510(k) records and may lag recent clearances. Always confirm status with the manufacturer before purchase.
Treatment economics
Economics data for this platform hasn't been published yet.
Chains using this device
No confirmed chain deployments recorded yet.
Owner reviews
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Alternatives
History
Every tracked change to pricing, lifecycle status, FDA data and warranty terms — newest first.
August 1, 2026
Record created
Added to The Aesthetic Index — August 2026
Source: The Aesthetic Index editorial
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