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LifeNet Health Northwest: FDA-registered device maker in Renton, WA, United States, 2 510(k) clearances

Name: LifeNet Health Northwest FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

LifeNet Health Northwest is registered with the FDA (registration 3009672666) in Renton, WA, United States. It lists 5 device types. The FDA files 2 510(k) clearances under its listings, the newest dated October 17, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3009672666
Address: 501 Sw 39th St, Renton, WA, United States, 98057
Owner or operator: LIFENET HEALTH (9079121)
Roles: Contract manufacturer, Manufacturer
First device listed: December 29, 2005
Registered through: 2026
Brand names listed: CardioGRAFT-MC Decellularized Pulmonary Artery Patch, FlexiGRAFT Connect, FlexiGRAFT Connect EXT, FlexiGRAFT DualLink, FlexiGRAFT GraftLink, FlexiGRAFT GraftLink TS, FlexiGRAFT QuadLink, FlexiGRAFT Sutured Lateral Ankle Tendon Construct and more

Devices it lists

Device	Product code	Class	Role	Source
Filler, Bone Void, Calcium Compound	MQV	2	Manufacturer	accessdata.fda.gov
Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)	MBP	2	Manufacturer	accessdata.fda.gov
Motor, Surgical Instrument, Ac-Powered	GEY	1	Contract manufacturer	accessdata.fda.gov
Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene	DXZ	2	Manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polyethylene	GAT	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
October 17, 2008	K081438	MATRACELL DECELLULARIZED PULMONARY ARTERY PATCH ALLOGRAFT	DXZ	Substantially Equivalent	Lifenet Health	accessdata.fda.gov
November 28, 2005	K053098	OPTIUM DBM GEL AND PUTTY	MBP	Substantially Equivalent	Lifenet	accessdata.fda.gov

Compare with other makers

Updated October 17, 2008. 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.