Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2183615

FEI Number

2183615

Entity Name

LIFE CORPORATION

City/State/Country

Orlando, FL, US

Establishment Address

2200 Principal Row, Orlando, FL 32837, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Applied Home Healthcare Equipment (Owner Number: 10033565)

Owner / Operator Contact Address

28825 Ranney Parkway, Westlake, OH 44145, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

One-Way Valve LIFE Mask; LIFE® CPR Mask LIFE OxygenPac; LIFE SoftPac; LIFE StartSystem; LIFE-O2; LIFE® Cannula, LIFE® PREP LIFE ® Cylinders; LIFE Cylinder & Cylinder Assembly; LIFE OxygenPac; LIFE SoftPac; LIFE StartSystem; LIFE-O2, LIFE® PREP OxyHome OxyGo Portable Oxygen Concentrator (1400-7000) Emergency Oxygen:LIFE OxygenPac;LIFE Regulator;LIFE SoftPac;LIFE StartSystem;LIFE-O2;LIFE OxygenPac;LIFE Soft;LIFE PREP

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CBP	Valve, Non-Rebreathing	Anesthesiology	Class 2	868.5870	2021-12-23
BYG	Mask, Oxygen	Anesthesiology	Class 1	868.5580	2021-12-23
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2021-12-23
ECX	Cylinder, Compressed Gas, And Valve	Anesthesiology	Class 1	868.2700	2021-12-23
CAW	Generator, Oxygen, Portable	Anesthesiology	Class 2	868.5440	2023-03-24
CAW	Generator, Oxygen, Portable	Anesthesiology	Class 2	868.5440	2026-05-06
CAN	Regulator, Pressure, Gas Cylinder	Anesthesiology	Class 1	868.2700	2021-12-23

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Applied Home Healthcare Equipment

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
K945177	Eagle Health Supplies	4-O2 JR. (CPR MOUTH BARRIER)	1994-11-01
K003939	Invacare Corp.	VENTURE HOME FILL II, MODEL IOH 200	2001-03-21
K942357	Healthdyne, Inc.	H-500 ALLIANCE OXYGEN CONCENTRATOR	1994-05-27
K042262	Sequal Technologies, Inc.	INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10	2004-09-10
K003472	Sequal Technologies, Inc.	INTEGRA OXYGEN CONCENTRATORS MODEL 6400-OM	2001-06-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0038-2007	Sunrise Medical	2	DeVilbiss iFill Personal Oxygen Station model number 535D.
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.

Similar Registrations

Registration Number	Establishment Name	Location
3014527907	WORLD SOURCE SIMPLE LLC.	Lima, OH, US
3004993040	LAERDAL MEDICAL (SUZHOU) CO., LTD.	215009 SUZHOU JIANGSU PROVINCE, CN
3013226	NORMED	SEATTLE, WA, US
8030673	PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.	MEXICALI Baja California, MX
3012307300	ICU Medical, Inc.	Minneapolis, MN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2183615. Last updated year: 2026. Please use registration number 2183615 when referencing this establishment in official correspondence.