Technology for your practice.
People by your side.
For doctors. For clinics. For the long run.
Your patients depend on your judgment. Your practice deserves a technology partner who supports it—with professional aesthetic devices, practical education, and ongoing technical service.
A partner in your practice
You focus on patients.
We help with the technology.
Choosing a device is only the beginning. For physicians, clinic owners, and their teams, the questions that follow matter just as much: Is it right for our practice? How will we learn it? Who can we call?
Start with your practice.
Explore devices by intended application, configuration, and the needs of your team. Discuss product documentation and available options with a specialist.
Explore Devices 02 Prepare your teamMake learning part of the plan.
Connect product education, onboarding, and continued learning with the people who will use your technology every day.
Explore Education 03 Stay connectedKnow where to turn.
Keep a direct connection to Apolomed for technical questions, maintenance needs, and support beyond installation.
Service & Support
Our Story
Founded in 2001, Apolomed (Shanghai Apolo Medical Technology) is a global manufacturer of medical aesthetic technology trusted by distributors, clinics, and enterprise partners worldwide. Operating from a modern manufacturing and R&D facility of more than 135,000 square feet in Shanghai, we specialize in the research, development, manufacturing, marketing, and long-term service of energy based medical systems.
We work with practices, distributors, and healthcare organizations on device selection, market-specific documentation, product education, and ongoing service. With dedicated service centers in New York and Toronto, Apolomed is not just a manufacturer. We are a long term technology partner committed to supporting our customers before, during, and after every installation.
Watch VideoIntegrated Manufacturing and Quality Control
Apolomed's manufacturing operation brings production, engineering, and quality assurance together in one organization.
Systems follow defined manufacturing and quality-control procedures before release. Available documentation depends on the model and market.
Global Reach, Regional Support
Apolomed technologies are trusted in over eighty countries and adopted by more than one hundred fifty companies worldwide, supported by a well-established international distributor network across North and South America, Europe, the Middle East, Oceania, and Asia.
Product availability, documentation, and service options vary by region. Contact the appropriate Apolomed team for current market-specific information.
Partnership, Service, and Support
Apolomed supports distributors and providers before, during, and after installation through product training, education, and technical service.
North American customers can contact the U.S. team in New York for sales and service support.
Explore Service and SupportShanghai origins. A continuing story.
Company History and Milestones
Explore the milestones behind Apolomed—from Shanghai Apolo's early development to expanded manufacturing, new aesthetic platforms and regional support for doctors and clinics.
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2001Our originsFounded in Shanghai
Shanghai Apolo's predecessor company was established, beginning a long-term commitment to medical-aesthetic technology.
Company historyCompany facility photo -
2009U.S. market pathwayPreparing for the U.S. market
FDA received the iPulseLight IPL 510(k) submission on November 23, 2009. This was a submission milestone—not clearance; clearance followed in January 2011.
FDA K093627Company facility collage; contextual -
2011Device clearanceAn IPL milestone in the U.S.
FDA 510(k) clearance for the iPulseLight IPL systems, models HS 300C and HS 650.
FDA K093627Company archive showroom photo -
2011Early 2011 · Company-reportedExpanding laser technologies
The company’s global history lists 1064 nm long-pulse, 1540 nm Er:Glass and 2940 nm Er:YAG laser systems in early 2011.
Company historyCompany production-line photo; contextual -
2014Company developmentA new corporate milestone
Listed on the Shanghai Equity Exchange under stock code 100243.
Company announcementCompany reception photo -
2015RecognitionHigh-tech enterprise recognition
Recognized as a High-Tech Enterprise in Shanghai—a milestone in the company's technology development.
Manufacturer historyCompany workshop photo -
2016Company-reported historyQuality-system milestones
Shanghai Apolo’s published history records CE marking and ISO 13485 certification through TÜV Rheinland. Later dated certificates are documented separately below.
Manufacturer historyCompany assembly team photo -
2017Technology developmentPicosecond platform introduced
Launched the HS-298 picosecond laser system.
Manufacturer historyManufacturer HS-298 product image -
2018Product registrationDiode system included in the ARTG
A diode laser hair-removal system manufactured by Shanghai Apolo was included in Australia’s ARTG on December 7, under entry 312300. The sponsor is Brand New Clinic Pty Ltd.
TGA ARTG 312300Company exhibition photo -
2018Materials testingRoHS testing by CCIC
CCIC issued RoHS test verifications for submitted HS-900 and HS-290/290E samples in July, and HS-770 in August. These records concern restricted-substance testing—not clinical performance.
View published documentCCIC test verification, 2018; published document -
2019Device clearanceDiode laser clearance
U.S. FDA 510(k) clearance for the 980 nm Diode Laser Therapy Device.
FDA K191349Shanghai company offices -
2019Materials assessmentSGS RoHS assessments
SGS issued RoHS certificates on February 13 for specified diode, IPL and Nd:YAG systems. The published certificates record validity through February 12, 2025; this is a historical milestone.
View published documentSGS certificate CN/19/00003; published document -
2020Device clearanceCO₂ laser clearance
U.S. FDA 510(k) clearance for the CO₂ Laser Therapy System.
FDA K201109Manufacturer CO₂ product image; contextual -
2020European conformity pathwayTÜV medical-device certificate
TÜV Rheinland issued EC certificate HD 60145599 0001 on March 31 under the Medical Devices Directive, Annex II excluding section 4, covering the listed device families and quality-assurance system.
View published documentTÜV EC certificate, 2020; published document -
2021Product registrationHS 510 included in the ARTG
The ApoloMed HS 510 HIFU system was included in the Australian Register of Therapeutic Goods.
TGA ARTG 357130Company archive reception photo -
2021Quality managementISO 13485 certificate issued
TÜV Rheinland issued certificate SX 2058336-1 in December for Shanghai Apolo’s medical-device quality-management system. This documented issue is part of the company’s certification history—not a claim of first certification.
View published documentISO 13485 certificate, 2021; published document -
2022Technology developmentDual-pulse platform introduced
Launched the HS-298N picosecond and nanosecond laser system.
Manufacturer historyManufacturer HS-298N product image -
2023Manufacturing growthExpanded Shanghai manufacturing
Relocated to a facility exceeding 7,500 m² and introduced updated sheet-metal product enclosures.
Manufacturer historyCompany manufacturing photo -
2024Development & productionMore room for what's next
Introduced the HS-232 system and expanded facilities to more than 12,500 m².
Manufacturer historyManufacturer HS-232 product image -
2024Quality-system auditMDSAP certificate issued
TÜV Rheinland issued MDSAP certificate MD 2058336-1-1 on April 15, with a stated expiry of April 14, 2027. It covers the specified quality-system scope; it does not grant every product approval in participating countries.
View published documentMDSAP certificate, 2024; published document -
2024European regulatory transitionMDR transition confirmed
On April 25, TÜV Rheinland confirmed a formal MDR application, written agreement and surveillance arrangements for listed devices under EU transition provisions. This confirmation letter is not an MDR certificate.
View published documentTÜV confirmation letter, 2024; published document -
2024Quality managementISO 13485 certification renewed
The December 30 ISO 13485 certificate lists Shanghai Apolo’s Nanle Road facility and replaces the November 2023 issue. It records validity through December 28, 2027 for the specified medical-device quality-management scope.
View published documentISO 13485 certificate, 2024; published document -
2025Regional supportCloser to North American practices
Opened the U.S. distribution and service center in Long Island, New York.
Explore service & supportShanghai company dispatch area -
2025Device clearanceA further fiber-laser milestone
U.S. FDA 510(k) clearance for Fiber Laser Treatment Systems HS-232 and HS-233.
FDA K251031Manufacturer HS-233 product image -
2026New systemsApolo One & PhotoVive
Released the new Apolo One and PhotoVive systems, expanding the Apolomed portfolio for doctors and clinics.
Explore our systemsCompany showroom photo -
2026Digital practice toolsIntroducing Apolomed Select
Introduced Apolomed Select to help patients and practitioners explore treatment and device options.
Read the announcementIllustrative optical artwork -
202625 yearsA quarter-century of development
Marking 25 years since the company's Shanghai origins in 2001. A continuing commitment to technology, education, and support.
Connect with our teamCompany exhibition & factory collage
Company photographs illustrate our facilities and work; they are not dated records of the events shown. Optical backgrounds are AI-created decorative artwork. Regulatory milestones apply to the named devices, entities and markets—not every Apolomed product. Company-reported milestones are identified above; contact us for current documentation.
Apolomed Pro: continued learning
Our education platform is being developed and introduced in phases, extending device-specific learning and support beyond initial training.
Explore Apolomed ProSupport for Canadian practices
Our Toronto service center is part of our regional support network. Contact the team for available services and device-specific support.
Explore regional supportResearch & technology development
Research and development remain part of Shanghai Apolo's work. Explore our research resources for study-specific methods, findings and limitations.
Explore research resources
Quality Management and Regulatory Documentation
Apolomed maintains quality-management processes for product development, manufacturing, and service.
Regulatory status varies by model and market. Review the product-specific documentation or contact Apolomed for current information before purchase or distribution.
Review CertificationsProducts for Practice and Portfolio Growth
Compare Apolomed aesthetic systems by modality, treatment application, available configurations, and support options.
Available indications, configurations, and regulatory status vary by device and market. A device specialist can help identify options for your practice or distribution portfolio.
Compare Devices
Events and Industry Engagement
Apolomed participates in international medical and aesthetic exhibitions, meetings, and educational forums.
These events give practices and distribution partners opportunities to meet the team, review products, and discuss market needs.
View EventsApolomed Pro
The next chapter
is continued learning.
Give education a lasting place in your practice. Explore Apolomed Pro and the training resources being developed for Apolomed device owners and their teams.
Discover Apolomed ProIncluded with your device.
Apolomed Pro is free with every purchased Apolomed device during that device’s warranty period.
Portal features and training content are being introduced in phases. Visit Education for the current overview and contact our team about access and device-specific availability.
Ready to Compare Devices?
Tell us which treatments or devices you are evaluating, and a specialist can help you compare options.