For the attention of: the medical director, lead physician, or principal of Beverly Hills Aesthetic Institute. If you are not the recipient above, please forward this link to them today.
Expires  May 30, 2026
Official Provider Invitation

Beverly Hills Aesthetic Institute has been pre-approved to offer Endolift® in Beverly Hills.

Following a structured review of aesthetic practices in the Los Angeles metro area, MediPrisma LLC has identified your practice as meeting the full set of criteria required for Endolift® provider status.

This invitation is personalized, time-limited, and non-transferable. It gives your practice direct access to the clinical pack, device evaluation pathway, and provisional position on the Beverly Hills provider shortlist.

Official Invitation
Invitation StatusPre-Approved
Issued ToBeverly Hills Aesthetic Institute
LocationBeverly Hills, CA
Issued OnApril 30, 2026
Expires OnMay 30, 2026
Issued ByMediPrisma LLC
Time Remaining
30
Days
00
Hours
00
Min
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Invitation at a glance

A new structural treatment tier for Beverly Hills Aesthetic Institute, and exclusive provider positioning in Beverly Hills.

The invitation gives your practice direct access to the evidence pack, device overview, training pathway, and Beverly Hills shortlist review.

Clinical pack

Protocol, published evidence, safety summaries, and patient-positioning materials.

Device evaluation

LASEmaR® 1500 overview, acquisition pathways, and medical-liaison call.

Training pathway

Provider onboarding, protocol review, and clinical implementation planning.

Market position

Shortlist consideration for the Beverly Hills provider territory.

Lower face treatment
Lower Face
Neck laxity treatment
Neck Laxity
Body contouring treatment
Body Contouring
The Procedure

Endolift® is a subdermal 1470nm laser procedure delivering selective adipolysis, immediate tissue contraction, and sustained collagen remodeling through a single-use optical fiber inserted beneath the skin surface. No incisions. Local anesthetic only. Outpatient setting.

The Commercial Position

Per-session fees in the US market range from $3,000 to $5,500. The procedure does not require a surgical suite, operates under local anesthetic, and uses single-use consumable fibers, yielding a margin profile consistent with premium injectable procedures.

Your Exclusivity

Endolift® invitations are issued to one practice per metropolitan area per cycle. Pre-approved status in Beverly Hills is specific to Beverly Hills Aesthetic Institute and cannot be transferred.

Before & After

Selected Endolift® results across face, neck, and body indications.

A curated gallery of representative before and after outcomes, presented in a clean carousel that fits the current brand style.

Endolift before and after result 1
Endolift before and after result 2
Endolift before and after result 3
Endolift before and after result 4
Endolift before and after result 5
Endolift before and after result 6
Endolift before and after result 7
Endolift before and after result 8
Endolift before and after result 9
Endolift before and after result 10
Endolift before and after result 11
Endolift before and after result 12
Endolift before and after result 13
Endolift before and after result 14
Why this practice was selected

Your practice passed our pre-approval review.

Before extending an invitation, our team conducts a structured review of aesthetic practices in each target area. We assess a defined set of criteria before any practice is shortlisted. Beverly Hills Aesthetic Institute met the threshold across all of the following.

Verified Clinical Credentials

The lead physician holds active board certification or equivalent clinical qualification in an aesthetic or medical specialty.

Established Patient Base

The practice has a documented patient volume consistent with successful integration of a premium procedure tier.

Positive Patient Reputation

Public review profile reflects consistently high patient satisfaction and clinical outcomes across multiple platforms.

Suitable Treatment Environment

The practice operates a compliant clinical facility appropriate for minor outpatient procedures under local anesthetic.

Aesthetic Procedure Portfolio

The practice already offers injectable, laser, or energy-based treatments, indicating an existing patient population suited to Endolift®.

Geographic Availability

No, or very few, other Endolift®-certified providers are currently operating within your immediate service area.

Pre-approval is reviewer-led, not automated. Each invitation is issued individually and tracked.

Your invitation is open for 30 more days. Beverly Hills Aesthetic Institute qualifies on every criterion above.

Clinical Mechanism

How Endolift® works, a subdermal laser platform that addresses tissue layers no surface-applied device can reach.

The LASEmaR® 1500 delivers 1470nm laser energy via a single-use optical fiber placed subdermally through a micro-entry point. The procedure addresses three simultaneous tissue targets through one session.

1
Subdermal Delivery

A micro-optical fiber delivers 1470nm laser energy through a small entry point.

2
Immediate Contraction

Thermal effect induces instant tissue contraction and hemostasis.

3
Collagen Stimulation

Neo-collagenesis and elastin remodeling continue over weeks to months.

4
Visible Results

Improved laxity, contour, and skin quality with minimal downtime.

Why 1470nm Specifically

At 1470nm, laser energy exhibits a water absorption coefficient approximately four times higher than at 980nm and significantly higher than 1064nm. This produces a narrower thermal zone with a steeper absorption gradient, enabling precise subdermal energy delivery.

LASEmaR 1500 device
Device Overview

LASEmaR® 1500

Engineered for precision. Designed for clinical confidence.
The LASEmaR® 1500 is a 1470nm diode laser platform purpose-built for minimally invasive aesthetic procedures.

Wavelength
1470 nm
Power
Up to 15W
Fiber
200 to 1000 microns
Indications
Face, neck, body
Downtime
Minimal, 2 to 5 days
The Clinical Position

Most non-surgical aesthetic platforms operate from the surface. Endolift® doesn't.

The treatment gap between injectable procedures and surgical intervention has been underserved by available technology. The table below positions Endolift® relative to the platforms already in your clinic.

TreatmentDepth of ActionFat ReductionCollagen StimulationAnestheticDowntime
RF MicroneedlingPartial subdermalLimitedModerateTopical2 to 5 days
HIFU / UltrasoundLimited subdermalNoModerateNoneMinimal
ThreadliftMechanical subdermalNoMildLocal3 to 7 days
External LaserSurface onlyNoSurface onlyNoneVaries
Surgical FaceliftFull subdermalPartialIncidentalGeneral / IV2 to 4 weeks
Endolift®Targeted subdermalYesStrong, histologically confirmedLocal2 to 5 days
Endolift® occupies the clinical space between injectable treatment and surgery. It addresses the structural tissue layer that no other non-surgical platform reaches, at outpatient cost and complexity.
The Patient Cohort

The patients you cannot fully serve today.

Within every established aesthetic practice, there is a patient cohort that presents beyond the ceiling of injectables but below the threshold, psychologically or clinically, for surgical referral. These patients are often highly loyal, treatment-experienced, and commercially valuable.

  • The patient between injectable ceiling and surgical threshold
  • The post-weight-loss patient with residual pockets and laxity
  • The patient who has plateaued on filler and is starting to look over-corrected
  • The early surgical candidate not yet ready for rhytidectomy
  • The localized fat presentation resistant to conservative measures
  • The atrophic acne scarring patient, rolling, boxcar, and icepick subtypes
Editorial clinical portrait
The Commercial Case

A premium structural procedure at outpatient operating cost.

The margin profile of Endolift® is determined by three variables: session fee, single-use consumable cost per fiber, and procedure time. The figures below are drawn from current US market data across certified providers.

$3,000–$5,500
Per-Session Fee
Typical US market range
20–25
Procedures to Typical Payback
Device acquisition, indicative
Month 1
Typical Net Revenue Established
Following training completion
Does Not Cannibalize

Endolift® serves a patient cohort your existing menu cannot reach. RF, HIFU, and injectable revenue is not displaced.

Premium Tier Positioning

The procedure's clinical complexity and device-driven delivery support premium price positioning.

Patient Retention

Providing a structural solution retains the treatment-ceiling patient within your practice.

Detailed acquisition options and finance pathways are in the Clinical Pack.

Market Demand

The procedure your patients are already searching for.

Consumer awareness of Endolift® has been driven by international press coverage across the past 24 months. Patient search volume is ahead of provider availability in most US markets.

Google Trends interest over time

Google Trends snapshot captured in April 2026, showing elevated U.S. search demand for Endolift® while local certified provider availability remains limited.

Vogue
Elle
Marie Claire
+ International Press
Patients searching "Endolift near me" in Beverly Hills today find limited or no certified options. Beverly Hills Aesthetic Institute's pre-approval places your practice at the front of this curve.
Clinical Evidence

Published clinical evidence includes peer-reviewed RCT, observational, and prospective data.

Randomized Controlled Trial
Bernardini et al., 2021. 96 subjects.

Prospective RCT evaluating Endolift® for facial and neck rejuvenation.

Prospective Observational
Tretti Clementoni et al., 2019.

Histological analysis confirms new collagen fiber formation and adipocyte disruption.

Histological Analysis
Multiple independent sites.

Serial biopsy data from treated and control sites.

Retrospective Cohort
Scuderi et al., 2022. Multi-center data.

Safety profile consistent with outpatient delivery and no serious adverse events attributable to the device.

Systematic Review
Independent review of 1470nm subdermal laser technology.

The full clinical evidence package, including all cited studies, methodology summaries, and safety data tables, is included in the Endolift® Clinical Pack.

Histological evidence of neo-collagenesis and elastin deposition is a consistent finding across independently conducted biopsy studies. All claims on this page refer to published data and do not constitute a guarantee of individual outcomes.

Provider Program

What is included with your pre-approved Endolift® provider package.

LASEmaR® 1500 device, compact desktop unit, fully configured
Single-use sterile fiber kit, RING (360°) and FLAT (directional) options
Comprehensive, supervised live clinical training at your practice
Official Endolift® practitioner certification on completion
A complete marketing kit, designed to launch fast
Listing in the public Endolift® practitioner directory
Endolift® Online Academy, clinical reference video library
Endolift® Practitioner Community, private peer network
Endolift® Masters Series, advanced technique training
Ongoing US-based clinical and commercial support from MediPrisma LLC
Acquisition note: Outright purchase and finance lease options available. Finance through Reliant Capital. Onboarding from confirmed acquisition to first independent patient treatment: typically 3 to 6 weeks depending on scheduling.
Time-Limited Invitation

Why your invitation is time-limited.

MediPrisma LLC issues Endolift® invitations on a rolling review cycle. Each cycle covers a defined geographic area, in this case the greater Beverly Hills metro, with a fixed number of provider slots. Pre-approval is valid for 30 days from issue. After expiration, the slot is released for the next review cycle. Approval in a later cycle is not guaranteed, because invitations are intentionally limited to preserve premium positioning and avoid oversaturating the market ahead of demand.

  • Pre-approval is specific to Beverly Hills Aesthetic Institute and cannot be transferred
  • One pre-approved invitation per practice per review cycle
  • Expired invitations require re-entry to the qualification review
  • Future cycles in Beverly Hills are not guaranteed within any specific timeframe

Your Beverly Hills window: 30 days remaining.

Next Steps

Accepting the invitation opens a structured evaluation pathway.

Submission is non-binding. Accepting places your practice on our confirmed contact list and triggers the clinical pack delivery. Nothing beyond that is assumed.

1

Receive the Clinical Pack

Delivered to your email within minutes. Full procedure overview, evidence summaries, device specifications, and commercial modeling.

2

Discuss Clinical Fit

Our US Medical Liaison contacts you within one business day. Indication selection, workflow integration, and menu positioning.

3

Review Acquisition Options

Purchase and finance pathways through Reliant Capital are walked through in detail. No pressure timeline.

4

Plan Training & Launch

Onboarding includes supervised training, certification, and launch support. First independent patient treatment typically within 3 to 6 weeks.

Talk to the team. Review the evidence. Understand the model. Then decide.

Practitioner Questions

Common questions from medical directors.

The pre-approval is reviewer-led and based on the six criteria listed on this page. Our team identifies practices in each target area using publicly available data: review profile, procedure portfolio, facility type, and geographic availability. Not every practice in the area receives an invitation.
The LASEmaR® 1500 is FDA-cleared under 510(k) reference K092860. It holds CE Mark Class IIb certification and is manufactured under ISO 13485 quality management standards at Eufoton® S.r.l., Trieste, Italy.
Training begins with a theory and protocol session covering anatomy, energy delivery parameters, indication selection, and contraindications. This is followed by supervised live clinical sessions with certification issued on confirmation of competence.
No. Endolift® serves a patient cohort that existing transcutaneous energy devices cannot reach, specifically those requiring subdermal fat reduction and structural tissue remodeling.
Published clinical data and real-world practice report typical downtime of 2 to 5 days, characterized by swelling and mild bruising at the entry point and treatment area.
Published multi-center retrospective data reports no serious adverse events attributable to the device at 6-month follow-up. Expected events include temporary swelling, bruising, and mild discomfort at the entry point.
Device pricing is provided directly during the acquisition conversation, not published on this page. Finance options through Reliant Capital are available for qualifying practices.
This invitation is addressed to the medical director, lead physician, or principal of Beverly Hills Aesthetic Institute. If you are not that person, please forward this page link directly to them today.
Accept Your Invitation

Accept your pre-approved Endolift® invitation.

Submit below to confirm interest. You will receive the Clinical Pack within minutes, a direct call from our US Medical Liaison within one business day, and provisional reservation of Beverly Hills Aesthetic Institute’s position on the Beverly Hills shortlist for 7 days.

For Medical Professionals only · Submission is non-binding · Your information is held by MediPrisma LLC and used solely to coordinate your Endolift® onboarding.

For Medical Professionals Only.

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PLEASE, BE ADVISED THAT IF YOU ARE NOT A MEDICAL PROFESSIONAL REGISTERED WITH THE GMC OR GDC, DO NOT SUBMIT AN INQUIRY. WE ARE NOT OFFERING TRAINING TO NON-MEDICAL PERSONNEL.

 

TRAINING WILL BE PROVIDED FOLLOWING THE PURCHASE OF EUFOTON LASEMAR 1500

* We DO NOT offer training to NMC, HCPC, or GPhC professionals.

Make an Enquiry

The Endolift® procedure is a cutting-edge, medical-only non-surgical laser treatment renowned for its remarkable ability to firm and tone the skin, effectively reducing laxity by retracting excess skin. In cases where necessary, ENDOLIFT® is also employed for reducing excessive fat and reshaping the face. It is often referred to as the gold standard in non- invasive skin tightening technology.
Ideal candidates for Endolift® are individuals with mild to moderate skin laxity on the face or body. This treatment is suitable for all skin types!
Endolift® stands as a distinct technology, often hailed as the non-invasive gold standard for achieving effective and long-lasting facelifts (skin tightening). Thanks to its thin probe, it can also be effectively used for tasks like acne scar subcision and cellulite subcision, yielding exceptional results.
Endolift® boasts a unique pedigree, developed by a team of experts over two decades ago. Attempts to replicate our technology can be found in the market, but our Fibres and Lasemar1500 devices remain unmatched in terms of efficacy and quality.
During the Endolift® procedure, a remarkably thin fibre-optic laser probe is inserted under the skin without the need for incisions. The laser energy is then carefully delivered to the deeper layers of the skin, stimulating collagen production and tightening the tissues. This controlled laser energy application kickstarts the body's natural healing process, resulting in skin tightening and improved texture. Additionally, the doctor can adjust the power to deliver enough energy to destroy adipose fat cells when required, which are then naturally eliminated by the lymphatic system.
Endolift® is commonly employed to treat areas of the face and neck that exhibit signs of aging, such as sagging skin, wrinkles, and loss of elasticity. It's often used to target the jawline, cheeks, nasolabial folds (smile lines), and the neck. Furthermore, it has proven highly effective in reducing localized fat in areas like the belly, inner thighs, bingo wings, and love handles.
The procedure is virtually painless. Local anesthesia is typically administered to numb the treatment area, minimizing any discomfort. While some patients may experience mild discomfort or a sensation of warmth during the procedure, it's generally not described as painful.
Endolift® triggers the natural production of structural proteins like collagen and elastin, resulting in improved skin 'architecture.' Early signs of improvement can often be observed within 4-8 weeks, with the process continuing over time. The peak results are usually realized 9-12 months after the procedure.
Yes, ENDOLIFT® is an FDA-approved minimally invasive outpatient laser procedure used in interstitial (endo-tissutal) aesthetic medicine. The laser treatment employs the latest Eufoton® LASEmaR® 1500, certified and approved by the American FDA for laser-assisted liposuction.
One of the primary benefits of Endolift® is its minimal downtime. Patients may experience some mild swelling, redness, and bruising in the treated area, typically subsiding within a few days to a week. Most patients can resume their normal activities shortly after the procedure.
The longevity of Endolift® results can vary from person to person. However, effects generally persist for several months to a few years. Maintenance treatments may be recommended to sustain results over time.
Endolift® is a skill-based procedure, exclusively performed by qualified medical practitioners who have undergone specialized training.
Endolift® results are both immediate and long-lasting. Following the treatment, results will continue to develop over several months as additional collagen forms in the deeper layers of the skin. Typically, these results can endure for 2 to 3 years, with the option to repeat the treatment after a year if desired.
The Endolift® procedure is a cutting-edge, medical-only non-surgical laser treatment renowned for its remarkable ability to firm and tone the skin, effectively reducing laxity by retracting excess skin. In cases where necessary, ENDOLIFT® is also employed for reducing excessive fat and reshaping the face. It is often referred to as the gold standard in non- invasive skin tightening technology.
Ideal candidates for Endolift® are individuals with mild to moderate skin laxity on the face or body. This treatment is suitable for all skin types!
Endolift® stands as a distinct technology, often hailed as the non-invasive gold standard for achieving effective and long-lasting facelifts (skin tightening). Thanks to its thin probe, it can also be effectively used for tasks like acne scar subcision and cellulite subcision, yielding exceptional results.
Endolift® boasts a unique pedigree, developed by a team of experts over two decades ago. Attempts to replicate our technology can be found in the market, but our Fibres and Lasemar1500 devices remain unmatched in terms of efficacy and quality.
During the Endolift® procedure, a remarkably thin fibre-optic laser probe is inserted under the skin without the need for incisions. The laser energy is then carefully delivered to the deeper layers of the skin, stimulating collagen production and tightening the tissues. This controlled laser energy application kickstarts the body's natural healing process, resulting in skin tightening and improved texture. Additionally, the doctor can adjust the power to deliver enough energy to destroy adipose fat cells when required, which are then naturally eliminated by the lymphatic system.
Endolift® is commonly employed to treat areas of the face and neck that exhibit signs of aging, such as sagging skin, wrinkles, and loss of elasticity. It's often used to target the jawline, cheeks, nasolabial folds (smile lines), and the neck. Furthermore, it has proven highly effective in reducing localized fat in areas like the belly, inner thighs, bingo wings, and love handles.
The procedure is virtually painless. Local anesthesia is typically administered to numb the treatment area, minimizing any discomfort. While some patients may experience mild discomfort or a sensation of warmth during the procedure, it's generally not described as painful.
Endolift® triggers the natural production of structural proteins like collagen and elastin, resulting in improved skin 'architecture.' Early signs of improvement can often be observed within 4-8 weeks, with the process continuing over time. The peak results are usually realized 9-12 months after the procedure.
Yes, ENDOLIFT® is an FDA-approved minimally invasive outpatient laser procedure used in interstitial (endo-tissutal) aesthetic medicine. The laser treatment employs the latest Eufoton® LASEmaR® 1500, certified and approved by the American FDA for laser-assisted liposuction.
One of the primary benefits of Endolift® is its minimal downtime. Patients may experience some mild swelling, redness, and bruising in the treated area, typically subsiding within a few days to a week. Most patients can resume their normal activities shortly after the procedure.
The longevity of Endolift® results can vary from person to person. However, effects generally persist for several months to a few years. Maintenance treatments may be recommended to sustain results over time.
Endolift® is a skill-based procedure, exclusively performed by qualified medical practitioners who have undergone specialized training.
Endolift® results are both immediate and long-lasting. Following the treatment, results will continue to develop over several months as additional collagen forms in the deeper layers of the skin. Typically, these results can endure for 2 to 3 years, with the option to repeat the treatment after a year if desired.

Make an Enquiry

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Please be advised we are offering training exclusively to our clients