# Korea Lifting Device Facts

> Find lifting device models, RF and ultrasound delivery systems, applicators and selected regulatory documents. Records retain the country, revision, source and matched Korean MFDS permit numbers.

## About the publisher

- Publisher: Korea Lifting Device Facts (https://kliftingdevices.site/)
- Nature: An editorial information project. Models are identified through source documents. No medical institution booking, referral or device sales service is provided.
- Other language: https://kliftingdevices.site/ko (한국 리프팅 기기 정보실)
- Contact: info@kliftingdevices.site

## Topic hubs

- [Lifting device types in Korea](https://kliftingdevices.site/topics/identity): Exact model, generation and applicator identify a device more precisely than its brand name alone.
- [Lifting energy types in Korea](https://kliftingdevices.site/topics/technology): RF, focused ultrasound and parallel-beam ultrasound describe different delivery architectures, with applicator-specific boundaries.
- [Lifting authorization checks](https://kliftingdevices.site/topics/regulation): A regulatory claim needs its own jurisdiction, exact model and indications document.
- [Device source provenance](https://kliftingdevices.site/topics/source-records): A source’s role and the extent actually read determine which device statements it can support.

## Statistics

- [Korea Oligio models](https://kliftingdevices.site/statistics/oligio-generation-records): Oligio, Oligio X and Oligio XM are separate records with different source and accessory relationships.
- [Korea surface RF devices](https://kliftingdevices.site/statistics/surface-rf-records): Surface RF records separate circuit, applicator and document scope rather than treating all RF brands as equivalent.
- [Korea DENSITY names](https://kliftingdevices.site/statistics/density-name-records): DENSITY, DENZA and DENSITY Noir appear together in one verified US submission, while the earlier DENSITY record remains separate.
- [Korea POTENZA tips](https://kliftingdevices.site/statistics/potenza-applicators): POTENZA includes documented needle and noninvasive applicators, so the handpiece and tip determine the penetration classification.
- [Korea InMode handpieces](https://kliftingdevices.site/statistics/inmode-handpiece-records): Forma / Plus and Morpheus8 use different RF applicators and retain separate indications within the selected InMode documents.
- [Korea Ulthera versions](https://kliftingdevices.site/statistics/ulthera-version-events): Ulthera legacy instructions, PRIME control units and later body-area events retain separate model and document revisions.
- [Korea Shurink model names](https://kliftingdevices.site/statistics/ultraformer-name-records): CLASSYS links Shurink to ULTRAFORMER III and Shurink Universe to ULTRAFORMER MPT, while local configuration and permit matches remain unresolved.
- [Korea Sofwave modules](https://kliftingdevices.site/statistics/sofwave-module-records): Sofwave SUPERB ultrasound and the Pure Impact electrical muscle-stimulation module have separate delivery and intended-use records.

## Tools (run in the browser, nothing stored)

- [Korea lifting model lookup](https://kliftingdevices.site/tools/model-finder): Match a device name to its documented model, energy and applicators while keeping Korean permit status unverified.
- [Korea device indication checks](https://kliftingdevices.site/tools/claim-checker): Compare a curated question with its exact jurisdiction, model and source rather than treating approval language as a universal claim.

## Articles

- [What does FDA clearance mean for a lifting device?](https://kliftingdevices.site/articles/clearance-and-approval): FDA clearance applies to the device and indications stated in its US document; it does not establish Korean authorization or superior lifting results.
- [How is a Korean device permit matched to a model?](https://kliftingdevices.site/articles/korean-permit-matching): A Korean permit match requires the exact domestic model and current permit records; a US letter or product introduction cannot fill that gap.
- [Why do RF frequency records differ across sources?](https://kliftingdevices.site/articles/frequency-conflicts): A conflicting specification remains a set of source-specific observations until model, source identity and document sections are matched.
- [Why identify the console, handpiece and tip?](https://kliftingdevices.site/articles/console-and-tip): The console, handpiece and tip identify different parts of a device configuration and can carry different source and use restrictions.
- [Where is ultrasound imaging documented in devices?](https://kliftingdevices.site/articles/imaging-identification): Ultrasound energy and ultrasound visualization are different fields, so imaging is recorded only when the source identifies it.
- [Do predicate devices share every indication?](https://kliftingdevices.site/articles/predicate-limits): A predicate supports the subject device’s substantial-equivalence submission, while the subject retains its own indications and restrictions.
- [Which models and lots does a device recall cover?](https://kliftingdevices.site/articles/recall-scope): A recall is matched to its jurisdiction, named product, catalog numbers and lots; a scoped accessory event does not describe every console.
- [What can a device UDI record identify?](https://kliftingdevices.site/articles/udi-is-not-an-indication): A UDI identity record can help match a model and labeler, while a device’s use scope remains tied to its own regulatory document.
- [Can an older device IFU show every current use?](https://kliftingdevices.site/articles/historical-ifu): An older instruction file records its own revision and scope, while later regulatory events remain separate records to match.
- [Does an unverified permit mean no authorization?](https://kliftingdevices.site/articles/unknown-is-not-unapproved): Unverified describes a missing research match, without proving permit absence, unavailability or unlawful individual use.

## Key pages

- [About device records](https://kliftingdevices.site/about)
- [Device record questions](https://kliftingdevices.site/faq)
- [Lifting device glossary](https://kliftingdevices.site/glossary)
- Feeds: https://kliftingdevices.site/rss.xml (RSS), https://kliftingdevices.site/feed.xml (Atom)
- Append /index.md to any page address for a Markdown copy: https://kliftingdevices.site/about/index.md

## Editorial rules

- Match the exact model and applicator.
- Read each record within its country and revision.
- Show Korean permits only from matched MFDS records.
- Regulatory decisions, manufacturer identity sources, original studies and reviews retain their distinct roles; first-party technical information is not independent clinical evidence.
- 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.