Data / Medical devices / Germany / Geske Beauty Tech GMBH
Geske Beauty Tech GMBH: FDA-registered device maker in Berlin, Germany, 1 510(k) clearance
Geske Beauty Tech GMBH is registered with the FDA (registration 3030052852) in Berlin, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 23, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030052852
- Address
- Leipziger Platz 18, Berlin, Germany, 10117
- Owner or operator
- GESKE Beauty Tech GmbH (10092696)
- Roles
- Complaint file establishment, Exporter to the US, Manufacturer, Specification developer
- First device listed
- May 30, 2025
- Registered through
- 2026
- Brand names listed
- MicroCurrent Face-Lift Pen 6 in 1 Aquamarine (REF: GK000907AQ02), MicroCurrent Face-Lift Pen 6 in 1 Black (REF: GK000907BK02), MicroCurrent Face-Lift Pen 6 in 1 Gray (REF: GK000907GY02), MicroCurrent Face-Lift Pen 6 in 1 Green (REF: GK000907GN02), MicroCurrent Face-Lift Pen 6 in 1 Magenta (REF: GK000907MG02), MicroCurrent Face-Lift Pen 6 in 1 Midnight (REF: GK000907MN02), MicroCurrent Face-Lift Pen 6 in 1 Pink (REF: GK000907PK02), MicroCurrent Face-Lift Pen 6 in 1 Purple (REF: GK000907PL02) and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Stimulator, Transcutaneous Electrical, Aesthetic Purposes | NFO | 2 | Complaint file establishment, Exporter to the US, Manufacturer, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 23, 2025 | K250361 | SmartAppGuidedTM MicroCurrent Face-Lift Pen 6 in 1 | NFO | Substantially Equivalent | Geske Beauty Tech GmbH | accessdata.fda.gov |
Compare with other makers
Updated May 23, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.