# Device record questions

> Model, accessory, jurisdiction and source role answer different device questions.

Use these distinctions when a commercial name, a clearance phrase or a recall headline leaves important conditions unstated.

Written by the Monun Device Research Group editorial team on October 25, 2026. Canonical address: https://kliftingdevices.site/faq.

## Which conditions help answer lifting device questions?

The exact name and accessory establish the record; country and revision establish the document scope.

A source can answer one question while leaving another unresolved. A model match can coexist with an unverified Korean permit, and a named recall can concern specified tips rather than every console. Those combinations remain visible rather than being compressed into a single yes or no.

## What else do people ask about lifting device questions?

### Why does Oligio appear in several records?

Original Oligio, X and XM retain generation and energy distinctions supported by their own sources.

### Can a brand name establish skin penetration?

A platform such as POTENZA has different applicator branches, so the exact tip is needed.

### Is Shurink Universe a matched Korean permit?

The manufacturer naming relation to MPT is documented, and MFDS permit 제허21-831호 lists ULTRAFORMER MPT with SHURINK UNIVERSE.

### Can one manufacturer’s indication be used for another device?

Each device keeps its own indications enclosure even when another device is used as a predicate.

### Does a new body-area event apply to every old console?

Model, revision, accessory and jurisdiction conditions need their own document match.

### Does a recall headline cover every product with that name?

A scoped record can name specific catalog numbers, tips and lots.

### Does no match mean no safety issue?

No match means absence from the selected collection, not a complete safety assessment.

### Can a specification establish the best device for my goal?

A technical value does not replace exact clinical endpoints, examination and personal consultation.

### Are ratings combined into a device score?

No patient-rating aggregation or invented score is part of the model and document collection.

## Where do these numbers come from?

- [K243929 : Oligio X](https://www.accessdata.fda.gov/cdrh_docs/pdf24/K243929.pdf) - U.S. Food and Drug Administration
- [K231287 : POTENZA](https://www.accessdata.fda.gov/cdrh_docs/pdf23/K231287.pdf) - U.S. Food and Drug Administration
- [Class 2 Device Recall XERF EFFECTOR 60](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=216122) - U.S. Food and Drug Administration
- [CLASSYS ESG Report 2022](https://one.classys.com/wp-content/uploads/2023/08/CLASSYS_Sustainability_Report_2022_ENG_vF-1.pdf) - CLASSYS
- [Medical device item search (의료기기안심책방): lifting device permits](https://emedi.mfds.go.kr/search/data/MNU20237) - Ministry of Food and Drug Safety