Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1000153536

FEI Number

1000153536

Entity Name

LIFEPORT, LLC.

City/State/Country

Woodland, WA, US

Establishment Address

1610 HERITAGE ST, Woodland, WA 98674, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LifePort (Owner Number: 10046674)

Owner / Operator Contact Address

1660 Heritage Street, Woodland, WA 98674, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NATO SIM Medical Divan Pole Mount MedDeck AeroSled Transport Deck (TD) Side Arch Litter Platform MedBed Twin Rotary Evacuation Carriage (TREC) Stretcher Deck Assembly Isolated Personnel Stacking Litter (IPSL) MedWall LifePort EpiShuttle Mounting Brackets ServiPlex AeroSled RS Turbo Utility Dual Patient Litter System (DPLS) Incubator Attachment Plates AeroSled Conversion Clip Deck Assembly Patient Loading Utility System (PLUS) Triple Litter Stacking System (TLSS) Arch Assembly Medical Cabinet Base Cabinet Assembly Ferno #9 Conversion Transition Deck Stacking Litter System (SLS) Over The Seat (OTS) Three Patient Litter System (TPLS) Cargo Sled ES Oxygen Module Assembly Equipment Mount Overhead Equipment Rack IV Pole Utility Pedestal Assembly Load Ramp Tower Assembly AeroSled Utility Deck (TD) Oxygen Shroud Stanchion Litter System (SLS) Medical Cabinet MedBed MedPak NATO SIM Patient Loading Utility System (PLUS) NATO SIM Utility Pedestal Assembly Medical Divan Medical Cabinet MedPak Twin Rotary Evacuation Carriage (TREC) Base Cabinet Assembly Patient Loading Utility System (PLUS) MedBed Powered Loading System (PLS) Medical Cabinet Medical Divan MedPak Oxygen Bottle Assembly Twin Rotary Evacuation Carriage (TREC) MedBed Oxygen Module Assembly NATO SIM Patient Loading Utility System (PLUS) Utility Pedestal Assembly Examination Light Medical Cabinet Belt Extender Assembly Footbag AeroSled Restraint Systems Belt Restraint Patient Loading Utility System (PLUS) MedBed Medical Divan MedPak Medical Cabinet NATO SIM Utility Pedestal Assembly Twin Rotary Evacuation Carriage (TREC)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FOX	Stand, Infusion	General Hospital	Class 1	880.6990	2014-11-26
BXO	Transducer, Gas Pressure	Anesthesiology	Class 1	868.2900	2019-12-16
BTI	Compressor, Air, Portable	Anesthesiology	Class 2	868.6250	2014-11-26
PCE	Permanently Mounted Wheelchair Platform Lift	Physical Medicine	Class 2	890.3930	2014-04-25
CAN	Regulator, Pressure, Gas Cylinder	Anesthesiology	Class 1	868.2700	2019-12-16
KZF	Device, Medical Examination, Ac Powered	General Hospital	Class 1	880.6320	2020-06-23
NZD	Stretcher, Patient Restraint	General Hospital	Class 1	880.6900	2019-12-16
GCX	Apparatus, Suction, Operating-Room, Wall Vacuum Powered	General Hospital	Class 2	880.6740	2014-11-26

Official Correspondent

Noah Zuckerman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LifePort

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K900686	Medical Industries America, Inc.	MAXI COMPRESSORS	1990-04-26
K851742	Burton Medical Products Corp.	MEDICAL EXAMINATION LIGHTS	1985-05-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0037-2010	Airgas Puritan Medical Puritan Medical Unit	1	AGI-2237 Portable 2 Cylinder Manifold Cart, for connecting medical gas cylinders.
Z-0038-2010	Airgas Puritan Medical Puritan Medical Unit	1	AGI-2238 Portable 4 Cylinder Manifold Cart, for connecting medical gas cylinders.

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3038623066	WUYI KINDA INDUSTRY & TRADE CO., LTD	JINHUA Zhejiang, CN
3008351005	Care&Care Health Products Co., Ltd	Yuanli Township Miaoli, TW

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000153536. Last updated year: 2026. Please use registration number 1000153536 when referencing this establishment in official correspondence.