Data / Medical devices / China / Suzhou Ahno Medical Devices Co., Ltd.

Suzhou Ahno Medical Devices Co., Ltd.: FDA-registered device maker in Suzhou Jiangsu, China, 2 510(k) clearances

Name: Suzhou Ahno Medical Devices Co., Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Suzhou Ahno Medical Devices Co., Ltd. is registered with the FDA (registration 3014315669) in Suzhou Jiangsu, China. It lists 17 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 3, 2014. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 3014315669
Address: Room B204 No. 8, Baoda Road Suzhou SIP, Suzhou Jiangsu, China, 215122
Owner or operator: Suzhou Ahno Medical Devices Co., Ltd. (10056864)
Roles: Contract manufacturer, Manufacturer
First device listed: January 24, 2018
Registered through: 2026

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Arthroscopic	NBH	1	Contract manufacturer	accessdata.fda.gov
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	KTT	2	Contract manufacturer	accessdata.fda.gov
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	LXT	2	Contract manufacturer	accessdata.fda.gov
Bit, Drill	HTW	1	Contract manufacturer	accessdata.fda.gov
Guide, Surgical, Instrument	FZX	1	Contract manufacturer	accessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	HWE	1	Contract manufacturer	accessdata.fda.gov
Intervertebral Fusion Device With Bone Graft, Lumbar	MAX	2	Contract manufacturer	accessdata.fda.gov
Orthopedic Manual Surgical Instrument	LXH	1	Contract manufacturer	accessdata.fda.gov
Pin, Fixation, Smooth	HTY	2	Contract manufacturer	accessdata.fda.gov
Pin, Fixation, Threaded	JDW	2	Contract manufacturer	accessdata.fda.gov
Plate, Fixation, Bone	HRS	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Prosthesis, Hip, Femoral Component, Cemented, Metal	JDG	2	Contract manufacturer	accessdata.fda.gov
Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer	HRY	2	Contract manufacturer	accessdata.fda.gov
Rod, Fixation, Intramedullary And Accessories	HSB	2	Contract manufacturer	accessdata.fda.gov
Screw, Fixation, Bone	HWC	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Template	HWT	1	Contract manufacturer	accessdata.fda.gov
Washer, Bolt Nut	HTN	2	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
June 3, 2014	K140891	BIOMET CANNULATED SCREW SYSTEM	HWC	Substantially Equivalent	Biomet, Inc.	accessdata.fda.gov
July 3, 2013	K131670	LAPIDUS PLATE, 3.5MM INLINE FUSION PLATE, 3.5MM MTP PLATE (LEFT AND RIGHT)	HRS	Substantially Equivalent	Biomet, Inc.	accessdata.fda.gov

Compare with other makers

Updated June 3, 2014. 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.