LifeNet Health Northwest

FDA Device Registration & Listing · Renton, WA, US · Registration 3009672666

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3009672666
FEI Number
3009672666
Entity Name
LifeNet Health Northwest
City/State/Country
Renton, WA, US
Establishment Address
501 Sw 39th St, Renton, WA 98057, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LIFENET HEALTH (Owner Number: 9079121)
Owner / Operator Contact Address
1864 CONCERT DR., --, VIRGINIA BEACH, VA 23453, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Optium DBM Vesuvius DBM Putty I/C Graft Chamber FlexiGRAFT GraftLink FlexiGRAFT Sutured Lateral Ankle Tendon Construct FlexiGRAFT GraftLink TS FlexiGRAFT Connect EXT FlexiGRAFT Connect FlexiGRAFT QuadLink FlexiGRAFT DualLink

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) Orthopedic Class 2 888.3045 2005-12-29
MQV Filler, Bone Void, Calcium Compound Orthopedic Class 2 888.3045 2005-12-29
GEY Motor, Surgical Instrument, Ac-Powered General, Plastic Surgery Class 1 878.4820 2013-01-30
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2007-08-27

Official Correspondent

MICHAEL PLEW

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIFENET HEALTH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005064037 LIFENET HEALTH Virginia Beach, VA, US
3005381997 LifeNet Health Virginia Bch, VA, US
3015724777 LifeNet Health Plainfield, IN, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K180121 Cellumed Co., Ltd. Rafugen DBM 2018-04-11
K062691 Takiron Co., Ltd. COMPORUS 2008-04-15
K023703 Berkeley Advanced Biomaterials, Inc. BI-OSTETIC 2003-01-30
K173933 Xenco Medical, LLC Sorrento Bioglass Bone Graft Substitute 2018-09-13
K905383 Micro Surgical Instruments Corp. 2710-000 OSCILLATING SAW, GENERAL ASSEMBLY 1991-06-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009672666. Last updated year: 2026. Please use registration number 3009672666 when referencing this establishment in official correspondence.
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