Data / Medical devices / China / Conod Medical Co., Ltd.

Conod Medical Co., Ltd.: FDA-registered device maker in Hangzhou Zhejiang, China, 1 510(k) clearance

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

Conod Medical Co., Ltd. is registered with the FDA (registration 3012568936) in Hangzhou Zhejiang, China. It lists 22 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 9, 2009. 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 Conod Medical Co., Ltd.

FDA registration number: 3012568936
Address: ROOM 2304, Haiyun International Building A Fuguangzhier Road, Hangzhou Zhejiang, China, 310000
Owner or operator: Conod Medical Co., Ltd. (10057159)
Roles: Exporter to the US
First device listed: March 1, 2018
Registered through: 2026
Brand names listed: 4 oz. Specimen Container w/Lid Non-Sterile; 800ml Urine/Stool specimen Collection, APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED, Adson forcep, BAG, URINARY LEG W/STRAPS, LEG BAG; Collector, Urine (And Accessories) For Indwelling catheter, Urinary drainageBag hold, Brush, Cleaning, Tracheal Tube, Bulb irrigation syringe 60cc ST; EAR Ulcer SYRINGE; Enteral irrigation syringe 60cc NS; Piston irrigation syringe, Convinient Kit; SHAVE PREP KIT; Skin Staple removal Kit; Suture Removal tray; Tracheostomy Care Trays; Irrigation tray, ENTERAL DELIVERY SET and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Catheter	KGZ	1	Exporter to the US	accessdata.fda.gov
Accessory, Surgical Apparel	LYU	1	Exporter to the US	accessdata.fda.gov
Apparatus, Suction, Single Patient Use, Portable, Nonpowered	GCY	1	Exporter to the US	accessdata.fda.gov
Bath, Sitz, Nonpowered	KTC	1	Exporter to the US	accessdata.fda.gov
Brush, Cleaning, Tracheal Tube	EPE	1	Exporter to the US	accessdata.fda.gov
Catheter And Tip, Suction	JOL	2	Exporter to the US	accessdata.fda.gov
Catheter Care Tray	OHR	2	Exporter to the US	accessdata.fda.gov
Collector, Urine, (And Accessories) For Indwelling Catheter	KNX	2	Exporter to the US	accessdata.fda.gov
Container, Specimen, Non-Sterile	NNI	1	Exporter to the US	accessdata.fda.gov
Container, Specimen, Sterile	FMH	1	Exporter to the US	accessdata.fda.gov
Device, Paste-On For Incontinence, Sterile	EXI	1	Exporter to the US	accessdata.fda.gov
Device, Urine Flow Rate Measuring, Non-Electrical, Disposable	FFG	2	Exporter to the US	accessdata.fda.gov
Enema Kit	FCE	1	Exporter to the US	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	Exporter to the US	accessdata.fda.gov
Forceps	HTD	1	Exporter to the US	accessdata.fda.gov
Holder, Ureteral Catheter	EYJ	1	Exporter to the US	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Exporter to the US	accessdata.fda.gov
Lubricant, Patient	KMJ	1	Exporter to the US	accessdata.fda.gov
Non-Surgical Gown	OEA	1	Exporter to the US	accessdata.fda.gov
Syringe, Irrigating (Non Dental)	KYZ	1	Exporter to the US	accessdata.fda.gov
Tube, Aspirating, Flexible, Connecting	BYY	2	Exporter to the US	accessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)	KNT	2	Exporter to the US	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
January 9, 2009	K082863	DYNAREX ENTERAL DELIVERY PUMP SET WITH SPIKE (1000ML), DYNAREX ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE (1000ML)	KNT	Substantially Equivalent	Dynarex Corporation	accessdata.fda.gov

Compare with other makers

Updated January 9, 2009. 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.