Search Results
Found 7 results
510(k) Data Aggregation
K Number
K242996Device Name
EndyMed PRO MAX
Manufacturer
EndyMed Medical Ltd.
Date Cleared
2025-06-10
(257 days)
Product Code
GEI, OUH, PBX
Regulation Number
878.4400Why did this record match?
Applicant Name (Manufacturer) :
EndyMed Medical Ltd
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The PRO MAX system is a Radiofrequency device intended for use in dermatologic procedures with separate indications for each handpiece.
The TC Handpieces (Shaper Max, Mini Shaper Max, iFine Max) are intended for:
• Relief of minor muscle aches and pain, relief of muscle spasm
• Temporary improvement of local blood circulation
When used up to 65W, the Mini Shaper Max and Small Max handpieces are also intended for the non-invasive treatment of mild to moderate facial wrinkles and rhytides.
The FSR Max Handpiece is intended for dermatological procedures requiring ablation and resurfacing of the skin.
The Intensif MAX Handpiece is intended for use in dermatologic procedures for electrocoagulation and hemostasis.
The EndyMed Contour MAX Handpiece is intended for the treatment of the following medical conditions; using the Contour MAX applicator for delivery of non-thermal RF combined with massage:
• Relief of minor muscle aches and pain, relief of muscle spasm
• Temporary improvement of local blood circulation
• Temporary reduction in the appearance of cellulite
Device Description
ENDYMED PRO™ MAX is a computerized system that generates pulses of radio frequency (RF) energy that are emitted onto patient skin. The device consists of a console and seven handpieces that emit either ablative or non-ablative radiofrequency.
Ask a Question
K Number
K161715Device Name
EndyGel
Manufacturer
EndyMed Medical Ltd.
Date Cleared
2017-02-07
(231 days)
Product Code
GYB
Regulation Number
882.1275Why did this record match?
Applicant Name (Manufacturer) :
EndyMed Medical Ltd
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Endy Gel is an Electroconductive gel media used with external electrode to reduce the impedance to alternating current) of the contact between the electrode surface and the skin.
Device Description
EndyMed's EndyGel™ is an Electroconductive gel media used with external electrode to enhance electrical conductivity by reducing the impedance (resistance to alternating current) of the radiofrequency signals path from the electrode surface between the electrode surface and the skin.
Ask a Question
K Number
K161199Device Name
EndyMed Contour Handpiece
Manufacturer
ENDYMED MEDICAL LTD.
Date Cleared
2016-08-01
(95 days)
Product Code
PBX
Regulation Number
878.4400Why did this record match?
Applicant Name (Manufacturer) :
ENDYMED MEDICAL LTD
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The EndyMed Contour Handpiece is intended for the treatment of the following medical conditions; using the Contour applicator for delivery of non-thermal RF combined with massage:
- · Relief of minor muscle aches and pain, relief of muscle spasm
- · Temporary improvement of local blood circulation
- · Temporary reduction in the appearance of cellulite.
Device Description
EndyMed's EndyMed Contour Handpiece is a treatment handpiece to be attached to the FDA cleared EndyMed Imagine TC Skin Treatment System (Imagine K08346). The EndyMed Contour Handpiece combines suction module that creates vacuum energy and emits bipolar RF energy that flows between the electrodes to create thermal heating of the tissue.
The Vacuum is used for the massaging of deep tissues by creating mild to deep suction. The vacuum massage contributes to the sub-dermal and adipose tissues shrinkage and improves the contact surface between electrodes and tissue.
Ask a Question
K Number
DEN150005Device Name
Newa Skin Therapy System
Manufacturer
EndyMed Medical Ltd.
Date Cleared
2015-12-18
(336 days)
Product Code
PAY
Regulation Number
878.4420Why did this record match?
Applicant Name (Manufacturer) :
EndyMed Medical Ltd
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The EndyMed Newa™ is an over-the-counter home use device intended for non-invasive treatment of mild to moderate facial wrinkles for adult women who have Fitzpatrick Skin Types I-IV.
Device Description
The Newa™ is an OTC, home use hand held device generating pulses of radiofrequency (RF) energy that are emitted into the skin. RF energy heats the tissue to improve the appearance of wrinkles and rhytides. It is a non-invasive, non-ablative device consisting of:
- User interface
- Programmable logic controller (PLC)
- RF power module
- Power supply
- RF electrodes
Ask a Question
K Number
K130501Device Name
INTENSIF
Manufacturer
ENDYMED MEDICAL LTD
Date Cleared
2014-03-13
(379 days)
Product Code
OUH, GEI
Regulation Number
878.4400Why did this record match?
Applicant Name (Manufacturer) :
ENDYMED MEDICAL LTD
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Intensif Applicator is intended for use in Dermatologic and General Surgical procedures for electrocoagulation and hemostasis.
Device Description
EndyMed's Intensif Applicator is a treatment handpiece to be attached to the FDA cleared EndyMed Imagine TC Skin Treatment System (K08346) (EndyMed Pro). The Intensif Applicator has a custom grid array of micro electrodes that is used to deliver the energy into the tissue. The Intensif Applicator tip emits bipolar RF energy that flows between electrodes to create thermal heating of the tissue for hemostasis and coagulation. The Intensif Applicator consists of: . Disposable treatment element (tip) . RF electrodes on a disposable tip . Operation trigger.
Ask a Question
K Number
K120513Device Name
GLOW BY ENDYMED
Manufacturer
ENDYMED MEDICAL LTD
Date Cleared
2012-05-08
(77 days)
Product Code
OUH, GEI
Regulation Number
878.4400Why did this record match?
Applicant Name (Manufacturer) :
ENDYMED MEDICAL LTD
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Glow by EndyMed is a noninvasive device intended for use in Dermatologic and General Surgical procedures. The TC applicator is indicated for mild to moderate facial wrinkles and rhytides. The FSR applicator is indicated for Dermatological procedures requiring ablation and resurfacing of the skin.
Device Description
The EndyMed Glow is a non-invasive unit consists of a user interface, programmable logic controller (PLC), an RF power module, internal electronics, and treatment handpieces. The user interface allows the selection of treatment parameters by pressing on the treatment buttons; A LCD screen displays the current treatment settings. The PLC is a specially configured computer that provides the operational and safety functions of the system. The system is connected to one or two out of 2 TC handpieces with different size electrode areas for different treatment sites, or to a FSR handpiece. The RF power module provides RF energy to the handpiece, producing a sinusoidal signal at 1MHz frequency.
Ask a Question
K Number
K101510Device Name
FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR
Manufacturer
ENDYMED MEDICAL LTD
Date Cleared
2011-02-17
(261 days)
Product Code
OUH
Regulation Number
878.4400Why did this record match?
Applicant Name (Manufacturer) :
ENDYMED MEDICAL LTD
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The Fractional Skin Resurfacing (FSR) Applicator is intended for dermatological procedures requiring ablation and resurfacing of the skin
Device Description
EndyMed's Fractional Skin Resurfacing (FSR) Applicator is a treatment handpiece to be attached to the FDA cleared EndyMed Imagine TC Skin Treatment System (K08346). The FSR Applicator tip emits bipolar RF energy that flows between electrodes to create micro-ablation points on the skin, forming superficial ablation with a volumetric non ablative heating effect in the dermis.
Ask a Question
Page 1 of 1