Data / Medical devices / China / Shun Sze Industrial (shenzhen) Co., Ltd

Shun Sze Industrial (shenzhen) Co., Ltd: FDA-registered device maker in SHENZHEN Guangdong, China, 1 510(k) clearance

Name: Shun Sze Industrial (shenzhen) Co., Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shun Sze Industrial (shenzhen) Co., Ltd is registered with the FDA (registration 3006542501) in SHENZHEN Guangdong, China. It lists 22 device types. The FDA files 1 510(k) clearance under its listings, the newest dated November 30, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3006542501
Address: No. 1, Jing Qiang Road Keng Zi, Pingshan District., SHENZHEN Guangdong, China, 518122
Owner or operator: SHUN HO INDUSTRIAL LTD. (9102463)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: June 4, 2007
Registered through: 2026
Brand names listed: 400563TG2 Target Finger Injury System 3/12, 67010, WKLY AM/PM PILL PLNR 6/72, 67010JC, JC WKLY AM/PM PILL PLNR 6/72, 67010TG2, TG AM/PM TRAVEL PILL PODS XL 6/72, 67010TG4 TGC AM/PM TRAVEL PILL PODS XL 6/72, 67012, POCKETTES PILL BOX 6/72, 67012HB,HEB POCKETTES PILL BOX 6/72, 67016, DAILY PILL PLANNER 6/72 and more

Devices it lists

Device	Product code	Class	Role	Source
Apparatus, Suction, Single Patient Use, Portable, Nonpowered	GCY	1	Contract manufacturer	accessdata.fda.gov
Applicator For Rectal Suppository	OOW	1	Contract manufacturer	accessdata.fda.gov
Applicator, Vaginal	HGD	1	Contract manufacturer	accessdata.fda.gov
Bag, Ice	KYR	1	Contract manufacturer	accessdata.fda.gov
Bottle, Hot/Cold Water	FPF	1	Contract manufacturer	accessdata.fda.gov
Case, Contact Lens	LRX	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Cup, Eye	LXQ	U	Contract manufacturer	accessdata.fda.gov
Depressor, Tongue, Non-Surgical	FMA	1	Contract manufacturer	accessdata.fda.gov
Dilator, Nasal	LWF	1	Contract manufacturer	accessdata.fda.gov
Dispenser, Liquid Medication	KYX	1	Contract manufacturer	accessdata.fda.gov
Dispenser, Solid Medication	NXB	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Douche Apparatus, Vaginal, Therapeutic	HED	1	Contract manufacturer	accessdata.fda.gov
Enema Kit	FCE	1	Contract manufacturer	accessdata.fda.gov
Mirror, Mouth	EAX	1	Contract manufacturer	accessdata.fda.gov
Nasal Spray, Ent Delivery	KCO	1	Contract manufacturer	accessdata.fda.gov
Pill Crusher/Cutter	OHY	1	Contract manufacturer	accessdata.fda.gov
Ring, Teething, Non-Fluid Filled	MEF	1	Contract manufacturer	accessdata.fda.gov
Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	HOY	1	Contract manufacturer, Manufacturer	accessdata.fda.gov
Speculum, Illuminated	FXF	1	Contract manufacturer	accessdata.fda.gov
Splint, Hand, And Components	ILH	1	Contract manufacturer, Manufacturer, Repackager or relabeler	accessdata.fda.gov
Syringe, Ent	KCP	1	Contract manufacturer	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Contract 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
November 30, 2017	K172925	Contact Lens Case, Model: A-1, B-1	LRX	Substantially Equivalent	P L Overseas Limited	accessdata.fda.gov

Compare with other makers

Updated November 30, 2017. 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.