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Company · CN

Shenzhen Osto Technology Company Limited

FDA 510(k) clearances and medical device recalls filed under this name, 2014 to 2022. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	10
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	1
OLP	Over-The-Counter Powered Light Based Laser For Acne	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Jul 7, 2022	K213056	LED Facial Mask Shenzhen Osto Technology Company Limited, CN	OLP
Dec 13, 2021	K211942	Heating Lumbar Therapy Cushion (Model: AST-622, AST-622B, AST-623, AST-623B) Shenzhen Osto Technology Company Limited, CN	NGX
Nov 22, 2021	K212989	Low-frequency Stimulator (Model: AST-645, AST-646) Shenzhen Osto Technology Co., Ltd., CN	NUH
Sep 5, 2021	K211736	Electronic Muscle Stimulator (Model: AST-300A, AST-300N, AST-300S, AST-300T, AST-300V, AST-300W) Shenzhen Osto Technology Company Limited, CN	NUH
Jun 11, 2021	K210756	Neck Care Therapy, Model: AST-905A, AST-905D, AST-905H Shenzhen Osto Technology Company Limited, CN	NUH
Mar 14, 2020	K190783	Health Expert Electronic Stimulator (model: AST-300L) Shenzhen Osto Technology Company Limited, CN	NUH
Dec 12, 2019	K190673	Health Expert Electronic Stimulator Shenzhen Osto Technology Company Limited, CN	NUH
Oct 10, 2019	K182136	Intelligent Wireless Fitness Apparatus (Model: AST-301, AST-302, AST-303) Shenzhen Osto Technology Co., Ltd., CN	NUH
Dec 7, 2018	K172897	Neck Care Therapy, Model: SYK 509B Shenzhen Osto Technology Co., Ltd., CN	NUH
Nov 26, 2018	K172837	Low-frequency Multi-function physiotherapy instrument Shenzhen Osto Technology Co., Ltd., CN	NUH
Sep 6, 2018	K172834	Dual output digital therapy massager Shenzhen Osto Technology Co., Ltd., CN	NUH
Nov 12, 2014	K133929	HEALTH EXPERT ELCTRONIC STIMULATOR Shenzhen Osto Technology Company Limited, CN	NUH

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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