Data / Medical devices / United States / Medicreations LLC

Medicreations LLC: FDA-registered device maker in Las Vegas, NV, United States, 8 510(k) clearances

Name: Medicreations LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Medicreations LLC is registered with the FDA (registration 3012772112) in Las Vegas, NV, United States. It lists 3 device types. The FDA files 8 510(k) clearances under its listings, the newest dated September 3, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3012772112
Address: 6370 Annie Oakley Dr., Las Vegas, NV, United States, 89120
Owner or operator: Medicreations LLC (10052855)
Roles: Manufacturer, Repackager or relabeler
First device listed: December 14, 2017
Registered through: 2026
Brand names listed: MediDiode, MediLight, MediSpa, MediYag, Velo

Devices it lists

Device	Product code	Class	Role	Source
Massager, Therapeutic, Electric	ISA	1	Manufacturer	accessdata.fda.gov
Powered Laser Surgical Instrument	GEX	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect	ONF	2	Manufacturer, Repackager or relabeler	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
September 3, 2025	K231952	MEDILIGHT	ONF	Substantially Equivalent	Medicreations, LLC	accessdata.fda.gov
December 20, 2024	K241670	Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2)	GEX	Substantially Equivalent	Beijing Adss Development Co., Ltd.	accessdata.fda.gov
October 9, 2024	K231948	MEDIYAG	GEX	Substantially Equivalent	Medicreations, LLC	accessdata.fda.gov
August 9, 2024	K231950	MEDIDIODE	GEX	Substantially Equivalent	Medicreations, LLC	accessdata.fda.gov
March 15, 2024	K233307	Intensity Pulsed Light Therapy System	ONF	Substantially Equivalent	Beijing Adss Development Co., Ltd.	accessdata.fda.gov
February 20, 2024	K231896	Diode Laser Therapy System	GEX	Substantially Equivalent	Beijing Adss Development Co., Ltd.	accessdata.fda.gov
February 22, 2017	K161926	ND YAG Q-switch Laser Therapy Machine	GEX	Substantially Equivalent	Beijing Adss Development Co., Ltd.	accessdata.fda.gov
October 5, 2016	K161925	CO2 Laser Therapy Machine	GEX	Substantially Equivalent	Beijing Adss Development Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 3, 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.