Korea Shurink model names
CLASSYS links Shurink to ULTRAFORMER III and Shurink Universe to ULTRAFORMER MPT, while local configuration and permit matches remain unresolved.
A naming relationship can help locate an English document without proving that every jurisdiction uses identical hardware and cartridges. The III and MPT source records remain separate.
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How do Shurink names connect to ULTRAFORMER?
The manufacturer’s corporate history provides the III / Shurink and MPT / Shurink Universe naming relationships.
The corporate report is a source for the manufacturer’s own naming statement. It helps a consumer connect Korean search terms to the product pages that use English names. It does not establish that each country’s model label, installed software or consumables are identical. Those are technical and regulatory matching questions.
| Exact record | Energy family | Verified US document and event date | Korean MFDS permit |
|---|---|---|---|
| ULTRAFORMER III | Ultrasound | No matched US event in this research | MFDS 제허14-1422호 (2014-08-01) |
| ULTRAFORMER MPT | Ultrasound | No matched US event in this research | MFDS 제허21-831호 (2021-10-06) |
Are ULTRAFORMER III and MPT one generation?
The manufacturer describes them as distinct product generations and gives MPT its own modes and cartridges.
A shared series name does not make every accessory interchangeable. The MPT page describes Normal and MP modes, while its own cartridge descriptions are retained with that product. A technical change described by the manufacturer is not, by itself, a comparative clinical result or a reason to rank treatments.
| Field | Confirmed source relationship | Still needs matching |
|---|---|---|
| Shurink | Manufacturer links the name to III | Exact domestic model and cartridge |
| Shurink Universe | Manufacturer links the name to MPT | Exact domestic label and revision |
| III / MPT | Distinct manufacturer product descriptions | Cross-market hardware and permit scope |
| MFDS public page | Historical III product information | Current product permit and amendments |
What energy do the ULTRAFORMER sources describe?
The manufacturer describes focused micro and macro ultrasound rather than RF delivery.
Focused ultrasound, imaging and a particular cartridge label are separate fields. The initial record did not verify an imaging function for these models, so it does not infer either imaging availability or a definite absence from the energy label. Manufacturer claims about an application also need their own authorization and clinical support.
What does the MFDS ULTRAFORMER III page establish?
The historical agency page names III and eyebrow lifting but is not a matched current permit detail.
A public product introduction can confirm what that institution published at that time. The page is not treated as a current attachment covering every marketed cartridge, body area or later MPT generation. Its role is retained as historical public information instead of being promoted to a complete present-day authorization list.
Why should a Shurink cartridge label remain visible?
The cartridge identifies an accessory configuration that cannot be recovered from the series name alone.
A list of cartridge options on a global product page is not a consumer instruction to choose a treatment depth. A local service label may describe only part of the configuration or bundle several components. The model finder retains the naming relationship while leaving unmatched local accessories explicit.
Can ULTRAFORMER marketing supply every permitted use?
Marketing describes the manufacturer’s claims; the applicable jurisdiction and exact product documents set the authorization question.
Examples about ampoules, skin quality or other applications on a global page are not entered as verified Korean indications. They also do not demonstrate that the source used an independent comparison. The catalog therefore uses product pages for model and technical identity and keeps therapeutic claims outside that source role.
Which Shurink fields remain unresolved?
Current domestic permits, exact local cartridge labels and cross-market equivalence remain unresolved.
No US event was matched for these records within the selected research. That gap does not establish that a device lacks every authorization, is unavailable locally or is ineffective. A consumer can still find the manufacturer naming sources and the historical agency page, with those limitations preserved next to the relationship.
A device name, US clearance or manufacturer description does not establish personal suitability or Korean authorization. These records are a dated source collection, not a complete clearance, recall or market inventory.
What else do people ask about Shurink model names?
Does Shurink Universe point to the MPT naming source?
Yes. The manufacturer names that relationship; it does not verify every country’s identical configuration.
Is III treated as another spelling of MPT?
The catalog preserves separate generation records.
Does the agency introduction replace a current permit?
It remains historical public product information, not a current permit attachment.
Does an ultrasound label prove imaging?
Imaging is a separate function and remains unverified in the selected records.
Does an unmatched US event mean unauthorized?
It means the selected research did not match that record; no legal-status conclusion follows.
Where do these numbers come from?
- ULTRAFORMER lll - CLASSYS Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. Product overview, HIFU/MMFU energy architecture; cartridge section and specification. No independent efficacy conclusion adopted.
- ULTRAFORMER MPT - CLASSYS Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. Product overview; HIFU architecture; Normal/MP modes; technical cartridge listing. Ampoule/drug-delivery marketing not treated as authorization.
- CLASSYS ESG Report 2022 Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. History excerpt page 8: Ultraformer III (Shurink); Ultraformer MPT (Shurink Universe). These are naming statements, not proof every jurisdiction shares identical hardware, software, cartridges or indications.
- Products | Medical Devices | Our Works | Ministry of Food and Drug Safety : CLASSYS Research access: 2026-10-24. Product section names Ultraformer III and intended use eyebrow lifting; registration/publication date 2016-03-31. Attachments and current permit status not read.
- Medical device item search (의료기기안심책방): lifting device permits Checked 2026-10-25 by product or model name. Permit number, holder, item, product and model name, permit date, validity and export-only flag were read from the item records. Attached technical documents were not read; model lists shown as 'and N more' were not expanded.