Korea Lifting Device Facts

Models, applicators and source documents · Research snapshot

Device topic directory

Published

Choose model identity, energy architecture, authorization scope or source provenance as your starting question.

The topic hubs connect all selected records and reading guides without creating a new page for every brand and body-area combination.

  • TopicLifting device types in Korea

    lifting device types: Oligio generations, DENSITY trade names and regional ultrasound names each have different evidence for their identity relationships.

  • TopicLifting energy types in Korea

    lifting energy types: Surface electrodes, penetrating pins, imaging transducers and muscle-stimulation modules should not be merged under one lifting label.

  • TopicLifting authorization checks

    lifting authorization checks: Selected US clearance records and Korean MFDS permits remain different fields. Later body-area events retain their own dates.

  • TopicDevice source provenance

    device source provenance: Regulator decisions, applicant summaries, manufacturer pages and original studies answer different questions.

Which lifting device topic fits the missing information?

Model identity, delivery architecture, authorization scope and source provenance are separate starting points.

A topic hub connects the records belonging to its question. Follow the identity hub when the name is unclear, or the source hub when the document is present but its role or reading extent is uncertain.

Where do these numbers come from?

  1. K243929 : Oligio X · US FDA 510(k) clearance (United States) · U.S. Food and Drug Administration · Primary source 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.
  2. K231287 : POTENZA · US FDA 510(k) clearance (United States) · U.S. Food and Drug Administration · Primary source 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.
  3. 의료기기안심책방 · Korea MFDS portal entry page · Ministry of Food and Drug Safety · Primary source Research access: 2026-10-24. Landing-page text only. Product-level search/permit attachments were not retrieved. No permit number or current Korea indication inferred.