Korea Oligio models
Oligio, Oligio X and Oligio XM are separate records with different source and accessory relationships.
A name on a quotation can identify a product family without identifying the exact console or tip. The original Oligio studies, the X regulatory events and the XM manufacturer description therefore remain separate.
On this page
Which Oligio models are recorded?
The original model, X and hybrid XM each have their own identity sources.
The original Oligio has a US record under The Oligio. Oligio X has separate US submissions, while the XM record comes from a Korean manufacturer product description. That source difference belongs next to each name, rather than being hidden behind one family label.
| Exact record | Energy family | Verified US document and event date | Korean MFDS permit |
|---|---|---|---|
| Oligio / The Oligio | Radiofrequency | K221989 (2022-10-13) | MFDS 제허20-396호 (2020-05-28) |
| Oligio X | Radiofrequency | K240313 (2024-02-22); K243929 (2025-01-21) | MFDS 제허23-860호 (2023-08-23) |
| Oligio XM | RF + ultrasound | No matched US event in this research | MFDS 제허23-885호 (2023-09-01) |
Does every Oligio model use the same energy?
The original and X records describe RF, while XM has separate RF tips and ultrasound cartridges.
The XM page describes a hybrid system. A combined console name does not make the RF and ultrasound applicators one interchangeable accessory. It also does not establish that the original Oligio clinical results apply to every XM mode.
| Field | Original / X | XM |
|---|---|---|
| Energy | RF | Manufacturer describes RF + ultrasound |
| Accessory | Surface RF tip | RF tip or ultrasound cartridge |
| Evidence transfer | Keep model-specific | No automatic transfer from original Oligio |
Why does Oligio X have more than one US record?
The catalog preserves the separate submission identifiers and their own document dates.
A regulatory event can address a model, a technical description or a change. The fact that both documents say Oligio X does not make the older file the full current instruction manual. Neither event dates Korean distribution or proves that a clinic is using the matched configuration.
How should conflicting Oligio X specifications be read?
Conflicting observations retain their source and scope instead of being averaged or silently replaced.
The FDA-filed and global manufacturer descriptions differ from a US-branded commercial page whose affiliation was not verified. The regulatory PDF also contains differing maximum-power descriptions in different sections. These are source-comparison questions, not grounds for a strongest-device ranking.
Is Oligio XM the same as Oligio KISS?
The manufacturer listing identifies KISS as an RF and HIFU lead, but cross-market equivalence with XM is unverified.
Shared energy words do not match hardware, software, cartridges or a legal model label. KISS remains outside the initial model records as a separate unresolved lead. A search result that uses the two names together cannot supply the missing regulator and label relationship.
Do the Oligio sources establish Korean authorization?
The verified US events and manufacturer pages do not supply matched current Korean permits.
A manufacturer footer can describe a purpose and an advertising review can have its own identifier. Neither is substituted for a matched product permit. Domestic verification still needs the exact label, permit attachment and amendments for the console and accessory in question.
What should be matched before reading Oligio results?
Match the console, tip, energy, study model and jurisdiction before connecting a result to a product.
A useful record of a quotation contains the exact model and accessory even when no personal information is entered. The model finder retrieves documented relationships; the claim checker displays the narrow regulatory scope. Neither function predicts treatment results or selects an energy setting.
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 Oligio models?
Does X mean XM?
No. They are separate records with different source and accessory relationships.
Can an original Oligio study prove XM results?
Not without a direct model and protocol match. The initial catalog makes no such transfer.
Is a US event a Korean launch date?
It dates a US regulatory event; Korean launch requires a different source.
Why is KISS not counted with XM?
The primary cross-market equivalence and labels have not been matched.
Can a frequency difference rank these models?
No. Source conflicts and different applicators do not support a performance ranking.
Where do these numbers come from?
- K221989 : The Oligio 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.
- K240313 : Oligio X Research access: 2026-10-24. Decision letter and indications-for-use enclosure. Four-page special-clearance document; no full device IFU.
- K243929 : Oligio X 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.
- wontech - products view Manufacturer first-party identity/technical source, not independent clinical evidence. Research access: 2026-10-24. OligioX identity; G/X modes; specifications 6.78 MHz, monopolar RF; cooling; comparison to earlier Oligio. Superiority wording not adopted.
- 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.
- Efficacy and Safety of Monopolar Radiofrequency for Treatment of Lower Facial Laxity in Asians Research access: 2026-10-24. Original full-text XML through Europe PMC: abstract, participants/design, device identity, full results/tables, acknowledgments/funding/disclosures read. Discussion/procedural instructions only selected passages; not a full-line read of every reference.
- Efficacy and Safety of Monopolar Radiofrequency for Tightening the Skin of Aged Faces Research access: 2026-10-24. Publisher full article in search extraction: abstract, design, device, outcomes/tables, limitations/discussion, funding/COI read; separate open returned 429. No graphical image audit.
- 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.