Data / Medical devices / Taiwan / I-Ming Sanitary Materials Co., Ltd.

I-Ming Sanitary Materials Co., Ltd.: FDA-registered device maker in Changhua, Taiwan, 1 510(k) clearance

Name: I-Ming Sanitary Materials Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

I-Ming Sanitary Materials Co., Ltd. is registered with the FDA (registration 9616933) in Changhua, Taiwan. It lists 27 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 3, 2010. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 9616933
FEI number: 3004755469
Address: No. 68, Sec. 2, Zhongke Erlin BLVD., Meifang Vil., Erlin Township, Changhua, Taiwan, 52666
Owner or operator: I-MING SANITARY MATERIALS CO., LTD. (9034430)
Roles: Manufacturer
First device listed: July 14, 1998
Registered through: 2026
Brand names listed: ABDOMINAL, ALINA, ARM, BAND OR BELT, BINDER, BREAST, Bandage, CAMELLIA and more

Devices it lists

Device	Product code	Class	Role	Source
Band Or Belt, Pelvic Support	ISR	1	Manufacturer	accessdata.fda.gov
Bandage, Elastic	FQM	1	Manufacturer	accessdata.fda.gov
Binder, Abdominal	FSD	1	Manufacturer	accessdata.fda.gov
Binder, Breast	HEF	1	Manufacturer	accessdata.fda.gov
Binder, Elastic	KMO	1	Manufacturer	accessdata.fda.gov
Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua	QKR	N	Manufacturer	accessdata.fda.gov
Insoles, Medical	KYS	1	Manufacturer	accessdata.fda.gov
Joint, Ankle, External Brace	ITW	1	Manufacturer	accessdata.fda.gov
Joint, Elbow, External Limb Component, Mechanical	IRD	1	Manufacturer	accessdata.fda.gov
Joint, Hip, External Brace	ITS	1	Manufacturer	accessdata.fda.gov
Joint, Knee, External Brace	ITQ	1	Manufacturer	accessdata.fda.gov
Orthosis, Cervical	IQK	1	Manufacturer	accessdata.fda.gov
Orthosis, Limb Brace	IQI	1	Manufacturer	accessdata.fda.gov
Orthosis, Lumbar	IQE	1	Manufacturer	accessdata.fda.gov
Orthosis, Lumbo-Sacral	IPY	1	Manufacturer	accessdata.fda.gov
Orthosis, Thoracic	IPT	1	Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Manufacturer	accessdata.fda.gov
Sleeve, Limb, Compressible	JOW	2	Manufacturer	accessdata.fda.gov
Sling, Arm	ILI	1	Manufacturer	accessdata.fda.gov
Splint, Clavicle	IQJ	1	Manufacturer	accessdata.fda.gov
Splint, Extremity, Noninflatable, External, Sterile	FYH	1	Manufacturer	accessdata.fda.gov
Splint, Hand, And Components	ILH	1	Manufacturer	accessdata.fda.gov
Splint, Temporary Training	IQM	1	Manufacturer	accessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)	FQL	1	Manufacturer	accessdata.fda.gov
Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)	DWL	2	Manufacturer	accessdata.fda.gov
Support, Arm	IOY	1	Manufacturer	accessdata.fda.gov
Support, Hernia	EXN	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
August 3, 2010	K092892	1-M GRADUATED COMPRESSION ANTI-EMBOLISM STOCKING, MODEL SS-811, SS-508, SS-613	DWL	Substantially Equivalent	I-Ming Sanitary Materials Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated August 3, 2010. 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.