Data / Medical devices / Hong Kong / Oman Medical Beauty Manufacture Limited

Oman Medical Beauty Manufacture Limited: FDA-registered device maker in Hong Kong, Hong Kong, 1 510(k) clearance

Name: Oman Medical Beauty Manufacture Limited FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Oman Medical Beauty Manufacture Limited is registered with the FDA (registration 3042228064) in Hong Kong, Hong Kong. It lists 18 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 25, 2024. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Oman Medical Beauty Manufacture Limited

FDA registration number: 3042228064
Address: Room B, 17/F, Run Kee Commercial Building, Shanghai Street, Mong Kok, Hong Kong, Hong Kong, 999077
Owner or operator: Oman Medical Beauty Manufacture Limited (10094349)
Roles: Contract manufacturer, Manufacturer
First device listed: November 24, 2025
Registered through: 2026
Brand names listed: 3D digital nail printer machine:MJY001,MJY002,MJY003,MJY004,MJY005,MJY006, Air pressure suit:AGF64,OMG61,OMG145,ksh68,OMG146,OMG147,OMG148,OMG149,OMG150,OMG-PST001,D03,OMD76,OM167,, BZY003,BZY004,BZY004,BZY005,BZY006,BZY007,BZY008,BZY009,BZY010,BZY011,BZY012,BZY013,, BZY014,BZY015,BZY016,BZY017,BZY018,BZY019,BZY020,BZY021,BZY022,BZY023,BZY024,BZY025,, BZY026,BZY027,BZY028,BZY029,BZY030,BZY031,BZY032,BZY033,BZY034, Body analyzer machine:C27,OM33,PFFX006,PFFX009,PFFX016, CLS30,CLS31,CLS32,CLS0033,CLS0037,CLS0038, CO2 and more

Devices it lists

Device	Product code	Class	Role	Source
Acetylcholine Chloride, Specific Reagent For Pseudo Cholinesterase	DLI	1	Manufacturer	accessdata.fda.gov
Bed, Manual	FNJ	1	Manufacturer	accessdata.fda.gov
Calculator/Data Processing Module, For Clinical Use	JQP	1	Manufacturer	accessdata.fda.gov
Colonic Irrigation System	KPL	2	Manufacturer	accessdata.fda.gov
Extracorporeal Shock Wave Device For Treatment Of Diabetic Foot Ulcers	PZL	2	Manufacturer	accessdata.fda.gov
Gas, Laser Generating	NXF	1	Manufacturer	accessdata.fda.gov
Guide, Needle, Surgical	GDF	1	Manufacturer	accessdata.fda.gov
Laser, Comb, Hair	OAP	2	Manufacturer	accessdata.fda.gov
Marker, Skin	FZZ	1	Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Manufacturer	accessdata.fda.gov
Powered Laser Surgical Instrument	GEX	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Powered Surgical Instrument For Improvement In The Appearance Of Cellulite	OUP	2	Manufacturer	accessdata.fda.gov
Stimulator, Muscle, Powered	IPF	2	Contract manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, For Pain Relief	GZJ	2	Manufacturer	accessdata.fda.gov
System, Imaging, Pulsed Doppler, Ultrasonic	IYN	2	Manufacturer	accessdata.fda.gov
Unit, Heating, Powered	IRQ	1	Manufacturer	accessdata.fda.gov
Unit, Syringe, Air And/Or Water	ECB	1	Manufacturer	accessdata.fda.gov
Vibrator, Therapeutic	IRO	1	Manufacturer	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 25, 2024	K241860	Diode Laser Hair Removal System	GEX	Substantially Equivalent	Beijing Winkonlaser Technology Limited	accessdata.fda.gov

Compare with other makers

Updated September 25, 2024. 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.