Korea lifting model lookup
Match a device name to its documented model, energy and applicators while keeping Korean permit status unverified.
Search a model or manufacturer, then inspect the accessory and source rather than treating a brand as one fixed treatment.
On this page
17 model / family records
- Oligio / The OligioWON TECH Co., Ltd.Original Oligio; exact Korean legal model not matchedEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허20-396호 (2020-05-28)
- Oligio XWON TECH Co., Ltd.Oligio X; two verified US clearance eventsEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허23-860호 (2023-08-23)
- Oligio XMWONTECH / 원텍 주식회사Korean marketed hybrid; exact regulatory model not matchedEnergy / applicatorRF + ultrasoundMatch the applicator and IFUKorean permitMFDS 제허23-885호 (2023-09-01)The permit lists the product name oligio xm and the model field Oligio Kiss plus one more. That places both names in one permit record; it does not establish that every configuration is identical.
- Thermage FLXSolta MedicalFLX; not CPTEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 수허18-245호 (2018-08-21)Thermage CPT has a separate permit (수허13-687호).
- VolnewmerCLASSYS Inc.Volnewmer; exact regional chassis/label pendingEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허22-512호 (2022-08-01)
- 10THERMATentech Inc.FDA model TMSY02Energy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허22-679호 (2022-10-11)The Korean model name (10THERMA-BK) differs from the US model TMSY02.
- DENSITY (2023 record)Jeisys Medical Inc.Original FDA Density record K230663Energy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허23-472호 (2023-04-05)
- DENSITY / DENZA / DENSITY Noir (2025 record)Jeisys Medical IncorporatedThree trade names explicitly listed in FDA K250065; not three independent devicesEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorDocumentsK250065 source, new tabKorean permitKorean permit unverifiedThe domestic DENSITY permit is 제허23-472호 (listed under the 2023 record). The DENSITY Noir permits found (제허23-63호, 제허24-114호) are export-only, and no DENZA permit was found, so the three-name 2025 record is not matched.
- POTENZAJeisys Medical Inc.K231287 update: S handpiece plus three noninvasive tipsEnergy / applicatorRadiofrequency (RF)Match the applicator and IFUSelect a tip to distinguish skin penetration.Korean permitMFDS 제허19-78호 (2019-01-29)Other POTENZA records (제허19-126호, 제허25-497호) are export-only. Tip electrodes are separate permits.
- XERFLutronic CorporationXERF K251327; exact Korea model pendingEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitMFDS 제허24-6호 (2024-01-03); MFDS 제허26-350호 (2026-05-11)Two domestic permits carry the XERF name; which one matches a given installed unit needs its label. XERF I and XERF-Overseas permits are export-only.
- Forma / Plus handpiecesInMode Ltd.Forma/Plus as configured on Optimas MAX; separate applicatorsEnergy / applicatorRadiofrequency (RF)Surface-contact applicatorKorean permitKorean permit unverifiedThe InMode RF import permit found (수허19-352호, model name Inmode RF) does not name Forma, so it is not matched.
- Morpheus8 applicator familyInMode Ltd.Morpheus8 applicators K231790; Optimas MAX configuration K251632; Burst/Cool branding is not automatic regulatory equivalenceEnergy / applicatorRadiofrequency (RF)Penetrating electrodesKorean permitKorean permit unverifiedThe InMode RF import permit found (수허19-352호, model name Inmode RF) does not name Morpheus8, so it is not matched.
- Ulthera System / Ultherapy (legacy IFU)Ulthera, Inc.Legacy control-unit IFU, 1015107IFU Rev 05Energy / applicatorUltrasoundSurface-contact applicatorKorean permitMFDS 수허09-1024호 (2009-10-13)One permit lists both Ulthera system and Ulthera Prime.
- Ulthera System PRIMEUlthera, Inc.UC-1 Control Unit PRIME K233996; PRIME Model 2.1 K250418 kept as model revisionEnergy / applicatorUltrasoundSurface-contact applicatorKorean permitMFDS 수허09-1024호 (2009-10-13)One permit lists both Ulthera system and Ulthera Prime.
- ULTRAFORMER IIICLASSYS Inc.ULTRAFORMER III; distinct from MPTEnergy / applicatorUltrasoundSurface-contact applicatorKorean permitMFDS 제허14-1422호 (2014-08-01)The ULTRAFORMER III UF3-C300 permit (제허19-201호) is export-only.
- ULTRAFORMER MPTCLASSYS Inc.MPT = Micro-Pulsed Technology; distinct from IIIEnergy / applicatorUltrasoundSurface-contact applicatorKorean permitMFDS 제허21-831호 (2021-10-06)ULTRAFORMER MPT PLUS has a separate permit (제허26-208호).
- SofWave System / SUPERBSofwave Medical Ltd.SUPERB ultrasound; Pure Impact is a separate electrical muscle-stimulation moduleEnergy / applicatorUltrasoundSurface-contact applicatorKorean permitMFDS 수허21-183호 (2021-07-22)
Research snapshot 2026-10-24; Korean permit numbers matched against MFDS item records on 2026-10-25. Not a list of Korean sales or installations. Inputs stay in browser memory.
Which names can lifting model lookup match?
The search matches documented model names, manufacturers and supported aliases from the identity snapshot.
A short commercial name can omit a generation or a module. Oligio, Oligio X and Oligio XM therefore keep separate records. The search uses text matching over those records, not an assessment of a photograph or a person. A result is a route to the documents behind the name.
Which fields appear in lifting model lookup?
Each match keeps the exact name, manufacturer, energy family, applicator state and source links together.
The initial collection contains 17 model or family records. That count describes this research collection, not the number of authorized or available devices in Korea. A source identifier opens the record supporting identity, and its role can be a regulator document or a manufacturer naming statement.
A blank Korean permit field is retained even when an overseas document has been matched. The two fields describe different jurisdictions.
| Field | Meaning | Unresolved condition |
|---|---|---|
| Name and generation | The record being matched | Domestic label may differ |
| Energy family | RF, ultrasound or a documented combination | Not an efficacy ranking |
| Korean permit | Separate domestic authorization field | Current permit and label not matched |
Why does lifting model lookup ask about the applicator?
A console can support applicators with different delivery methods, so skin penetration may depend on the selected tip.
POTENZA document K231287 includes microneedle electrodes and the S handpiece with noninvasive DDR, SFA and Diamond tips. With no tip selected, the tool keeps the mixed state. Selecting the documented noninvasive branch changes the displayed accessory description without changing the platform into a different device.
How does lifting model lookup handle regional aliases?
A manufacturer naming statement supports a name relationship but does not prove every regional configuration is identical.
CLASSYS describes Shurink Universe in relation to ULTRAFORMER MPT in its corporate naming record. That lets the search return the MPT identity. It does not establish interchangeable cartridges, identical software or a current Korean permit. Oligio KISS and XM remain an unresolved relationship because a shared energy description is insufficient to merge models.
| Input | Matched record | Boundary |
|---|---|---|
| Shurink Universe | ULTRAFORMER MPT | Manufacturer naming statement |
| POTENZA with no tip | POTENZA mixed applicators | Needle and noninvasive branches stay separate |
| Oligio XM / KISS | XM record; relationship unresolved | No automatic model merger |
What does the jurisdiction choice change in lifting model lookup?
The jurisdiction choice narrows document links; it does not transform an overseas record into Korean authorization.
US documents retain their FDA or US instruction-manual scope. The Korean lookup route points toward domestic verification while the permit field remains unresolved. No country choice determines whether a device is being sold, installed or used at a particular clinic. The list is not a current market inventory.
When was lifting model lookup data checked?
The identity collection uses the 2026-10-24 research snapshot and retains each source’s reading extent.
The search runs against the deployed snapshot rather than querying a regulator in real time. Source metadata distinguishes decision dates, research access and document revisions. Reading a selected indications section does not count as reading a complete instruction manual or every amendment.
What does lifting model lookup store or decide?
Inputs stay in browser memory; the tool matches documents without storing health information or selecting treatment.
No age, diagnosis, facial photograph or contact detail is needed. Search terms are not added to the URL or sent to a server by the tool. Opening an external source follows that publisher’s own website conditions. An unmatched name remains outside this collection rather than becoming a finding of unauthorized use.
What are the limits of this tool?
- Identity records do not select treatment or establish current Korean authorization.
- An omitted applicator remains unresolved when a platform supports different tips.
- The collection covers selected documents rather than every model or market.
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 basis are these numbers on?
| Snapshot | Source | Reference date | Retrieved | Site calculation |
|---|---|---|---|---|
| Model identities | U.S. Food and Drug Administration, Ministry of Food and Drug Safety, Original paper via NLM, U.S. Food and Drug Administration, American Academy of Dermatology, InMode, Original paper via NLM, InMode-branded regional website (India), InMode-branded regional website (Italy), U.S. Food and Drug Administration, U.S. Food and Drug Administration, Cynosure Lutronic, Korea Health Industry Development Institute (MFDS repost), Original paper via NLM, U.S. Food and Drug Administration, CLASSYS, WONTECH, WONTECH, U.S. Food and Drug Administration, WONTECH, Original paper via NLM, Original paper via NLM, Original paper via NLM, U.S. Food and Drug Administration, Ulthera : US instructions for use, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, WONTECH, Original paper via NLM, U.S. Food and Drug Administration, Original paper via NLM, Sofwave Medical, Original paper via NLM, Korea Consumer Agency, U.S. Food and Drug Administration, U.S. Food and Drug Administration, CLASSYS, Ministry of Food and Drug Safety, American Academy of Dermatology, American Academy of Dermatology, Korea Law Information Center, Solta Medical, CLASSYS, Cosmetics, Original paper via NLM, Original paper via NLM, Springer Nature, U.S. Food and Drug Administration, American Academy of Dermatology, U.S. Food and Drug Administration, WONTECH, U.S. Food and Drug Administration, Commercial website; corporate affiliation unverified, U.S. Food and Drug Administration, CLASSYS, U.S. Food and Drug Administration, U.S. Food and Drug Administration, Ulthera : US instructions for use, U.S. Food and Drug Administration, U.S. National Library of Medicine : AccessGUDID, U.S. Food and Drug Administration | October 24, 2026 | October 24, 2026 | - |
| Documented applicators | U.S. Food and Drug Administration, Ulthera : US instructions for use | October 24, 2026 | October 24, 2026 | - |
| Source provenance | U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, U.S. Food and Drug Administration, WONTECH, WONTECH, WONTECH, WONTECH, WONTECH, Commercial website; corporate affiliation unverified, Solta Medical, CLASSYS, CLASSYS, CLASSYS, CLASSYS, Ministry of Food and Drug Safety, Ministry of Food and Drug Safety, InMode-branded regional website (India), InMode, InMode-branded regional website (Italy), Ulthera : US instructions for use, Ulthera : US instructions for use, Sofwave Medical, Cynosure Lutronic, U.S. Food and Drug Administration, U.S. National Library of Medicine : AccessGUDID, Original paper via NLM, Cosmetics, Springer Nature, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, Original paper via NLM, U.S. Food and Drug Administration, U.S. Food and Drug Administration, Korea Health Industry Development Institute (MFDS repost), Korea Consumer Agency, American Academy of Dermatology, American Academy of Dermatology, American Academy of Dermatology, American Academy of Dermatology, Korea Law Information Center, U.S. Food and Drug Administration | October 24, 2026 | October 24, 2026 | - |
What else do people ask about lifting model lookup?
Can I search a Korean trade name?
Yes, when the identity record contains that Korean name or a documented alias.
Does one result prove it is the device on my quote?
The actual model and applicator label still need to match the quote.
Does a filter show all authorized devices?
No. It filters this selected research collection.
Why can an applicator remain unresolved?
The platform may support different delivery methods or the source may not establish the exact local accessory.
Does the finder compare expected results?
It compares identities and source relationships, not personal clinical outcomes.
Where do these numbers come from?
- K231287 : POTENZA Research access: 2026-10-24. Decision letter identity/date; indications-for-use enclosure and/or summary; device-description/technology sections. Selected sections only, not a full IFU or full dossier.
- 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.
- 올리지오xm | 고주파+초음파 멀티 에너지 리프팅 Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. Identity, RF G/X and ultrasound 3.0/4.5 modes, monopolar RF + ultrasound system type, RF tips and ultrasound cartridges; legal footer has separate coagulation and eyebrow-lift purposes. Advertising-review number is not used as a device permit.
- WONTECH Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. Product list identifies OligioKISS as HIFU & RF Device. Listing does not establish equivalence to Korean Oligio XM, permit or IFU.
- 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.