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Minimal Aesthetics

2024 InMode IgniteRF with Morpheus8 Burst & QuantumRF

$74,899.00
Shipping calculated at checkout.
Description
Specifications

Elevate your surgical and aesthetic offering with this 2024 InMode IgniteRF platform, configured with Morpheus8 Burst Face, Morpheus8 Burst Deep Body, and QuantumRF technology. Designed for advanced facial and body remodeling, this system gives plastic surgeons and luxury aesthetic practices a versatile RF platform for skin tightening, tissue remodeling, contour refinement, and deeper subdermal applications.

Morpheus8 Burst technology delivers radiofrequency energy across multiple tissue depths within a treatment cycle, allowing providers to customize procedures based on the treatment area, tissue thickness, and desired clinical endpoint. The Burst Face handpiece supports precision facial and smaller-area treatments, while the Burst Deep Body handpiece is designed for larger treatment zones and deeper tissue remodeling.

Device Includes: 
Base Unit
Morpheus 8 Burst Face Handpiece
Morpheus 8 Burst Deep Body Handpiece
Demo Tip
2 handpiece cradles
QuantumRF 10 disposable Handpiece
QuantumRF 25  disposable Handpiece 
Foot Pedal
Quick Reference Guides
Power Cord
Manual

QuantumRF expands the platform’s functionality with internally delivered fractional radiofrequency for controlled subdermal coagulation and tissue contraction. The QuantumRF 10 handpieces are suited for smaller, more precise treatment areas, while the QuantumRF 25 handpieces support broader face and body applications. Together, these technologies provide a comprehensive platform for practices offering advanced facial rejuvenation, skin tightening, body contouring, and surgical-adjacent aesthetic procedures.

 

MANUFACTURER
InMode Ltd.
COMMERCIAL DEVICE NAME
Ignite RF System
MODEL / CATALOG NUMBER
AG613237A
PRIMARY DEVICE IDENTIFIER (UDI-DI)
07290019863250
2024 FDA 510(K)
K240780
FDA DEVICE CLASSIFICATION
Class II — Electrosurgical cutting and coagulation device and accessories
FDA PRODUCT CODE
GEI
REGULATION NUMBER
21 CFR 878.4400
ENERGY MODALITY
Radiofrequency (RF)
SYSTEM ARCHITECTURE
Computerized RF energy system
PRIMARY CLINICAL FUNCTION
Electrocoagulation / contraction of soft tissue and hemostasis
FEEDBACK MECHANISMS
Integral temperature and impedance feedback
ENERGY CONTROL
Continuously monitors target-tissue temperature and impedance and automatically adjusts energy delivery
CONSOLE COMPONENTS
AC/DC power supply, RF generator, controller, and user interface
DISPLAY / INTERFACE
Touchscreen user interface
HANDPIECE CONNECTION
RF handpiece connects to console by cable
ENERGY ACTIVATION
Foot switch activates energy delivery to the handpiece
PREVIOUSLY CLEARED COMPATIBLE HANDPIECES
HP060909A; HP101306A; HP172206A; HP172246A; HP172248A; HP102206A; HP253966A
HANDPIECES ADDED UNDER K240780
HP1022B6A; HP2539B6A
ADDED HANDPIECE CONFIGURATION
Bipolar; 2 active internal electrodes; no external return electrode
THERMAL-EFFECT CONTROL FOR ADDED HANDPIECES
Controlled by selection of delivered amount of energy
TECHNOLOGY FAMILIES MARKETED FOR IGNITERF
QuantumRF, Morpheus8, and RFAL technologies
MAXIMUM MARKETED PENETRATION DEPTH
Up to 60 mm with compatible technology / applicator
FDA-CLEARED INDICATIONS FOR USE
Dermatological and general surgical procedures where coagulation/contraction of soft tissue or hemostasis is needed
PRESCRIPTION DEVICE
Yes
MEDICAL SPECIALTY
General & Plastic Surgery
FDA DECISION DATE FOR K240780
July 24, 2024
ELECTRICAL & MECHANICAL SAFETY TESTING
IEC 60601-1
ELECTROMAGNETIC COMPATIBILITY TESTING
IEC 60601-1-2
HIGH-FREQUENCY SURGICAL EQUIPMENT TESTING
IEC 60601-2-2
PERFORMANCE VERIFICATION
Software validation, electrical/mechanical safety, EMC, RF output testing, and comparative ex vivo tissue testing
Inmode Aesthetics  |  SKU: P-00284-L

Terms & Conditions

Training

We take pride in the unique value-added services we provide to our customers. With each purchase, we offer complimentary virtual clinical training, ensuring you understand the full potential of your investment. This comprehensive training, typically spanning two to four hours, covers a variety of crucial aspects - from indications and contra-indications to protocol, patient charting, and technique/application coaching. The goal is to empower you with the knowledge and skills to optimize your use of the purchased product. Moreover, each attendee is presented with a certificate of completion, testifying to their newfound expertise. If you require hands-on and onsite training, we can provide a custom quote to cater to your specific needs. Please note that product sales under $10,000.00 may have additional fees applied for training services.

Warranty

Each product purchased comes with a guarantee of minimum 90-day warranty starting from the delivery date. This warranty ensures that if any mechanical or technical issue arises that isn't caused by user error, the buyer can return the product for full repair or replacement. Please note, however, that the cost of return shipping will be borne by the buyer. We are committed to standing by our products; therefore, after the initial 90-day warranty period, all customers can avail our service at the cost of parts, in addition to a labor fee of $185.00 per hour, and any shipping fees incurred. Please not that product sales under $10,000.00 may have additional fees applied for training services.

Shipping

At our company, orders are set into motion as soon as they are fully funded. We take pride in ensuring that every product you purchase from us passes a rigorous final quality control inspection. Typically, this inspection happens within one to two business days following payment completion. Our team then proceeds to package each unit professionally, a process influenced by order volume and fulfillment queues. It's worth noting that this packaging step can take anywhere from three to five business days. Following packaging, your item is shipped, fully insured, via a reputable domestic or international carrier. Our standard shipping service provides a delivery timeline of three to five days. We value our international customers, and therefore, we make weekly international shipments, supported by our valid import and export licenses. Rest assured, we are committed to delivering quality and value, no matter where you are in the world. 

Returns

All purchases are subject to a final sale policy, ensuring that no refunds or exchanges are allowed under normal circumstances. Nonetheless, we understand that unexpected technical or mechanical issues can arise. Should you encounter such issues within the warranty period, we invite you to submit a service request form for our team to review. In cases where the request is approved, we will provide an RMA (Return Merchandise Authorization) number, allowing the return of the item for either repair or replacement. If you're interested in an extended warranty period, we would be glad to offer a quote for this additional service at an extra cost to your purchase.

Medical Device Acknowledgement

By signing below, Buyer/Customer agrees to and understands the following:

Federal (USA) law restricts (and state law may restrict) this medical device to sale or use by or

on the order of a physician, dentist, veterinarian or other practitioner licensed in the state in

which this medical device is used or ordered (a "Prescribing Practitioner"). Customer and

Customer's Prescribing Practitioner are solely responsible for the use and operation of this

medical device in accordance with all applicable laws and regulations, and medical and

treatment guidelines, and for ensuring that each operator of this medical device is adequately

trained and qualified to use and operate this medical device safely and properly in a clinical

setting and to perform medical procedures in accordance with such laws, regulations and

guidelines. Synergy Medsales makes no representations or warranties regarding federal,

state or local laws or regulations, or medical or treatment guidelines, that might apply to the use

and operation of this or any medical device. Customer and Customer's Prescribing Practitioner

are solely responsible for contacting state and local licensing agencies regarding requirements

applicable to the use and operation of this medical device. Use of this medical device involves

certain risks of injury to patients. Customer and Customer's Prescribing Practitioner are solely

responsible for ensuring that patients are informed of these risks. Improper use of this medical

device may increase the risk of injury to patients.