Data / Medical devices / United States / Life Corporation
Life Corporation: FDA-registered device maker in Orlando, FL, United States, 3 510(k) clearances
Life Corporation is registered with the FDA (registration 2183615) in Orlando, FL, United States. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 23, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2183615
- Address
- 2200 Principal Row, Orlando, FL, United States, 32837
- Owner or operator
- Applied Home Healthcare Equipment (10033565)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 23, 2021
- Registered through
- 2026
- Brand names listed
- Emergency Oxygen:LIFE OxygenPac;LIFE Regulator;LIFE SoftPac;LIFE StartSystem;LIFE-O2;LIFE OxygenPac;LIFE Soft;LIFE PREP, 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, One-Way Valve, OxyGo Portable Oxygen Concentrator (1400-7000), OxyHome
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Nasal, Oxygen | CAT | 1 | Manufacturer | accessdata.fda.gov |
| Cylinder, Compressed Gas, And Valve | ECX | 1 | Manufacturer | accessdata.fda.gov |
| Generator, Oxygen, Portable | CAW | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Mask, Oxygen | BYG | 1 | Manufacturer | accessdata.fda.gov |
| Regulator, Pressure, Gas Cylinder | CAN | 1 | Manufacturer | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| April 23, 2026 | K252407 | OxyGo Portable Oxygen Concentrator (1400-7000) | CAW | Substantially Equivalent | Mv Life, LLC | accessdata.fda.gov |
| July 20, 2020 | K191875 | Owgels Oxygen Concentrator | CAW | Substantially Equivalent | Guangzhou Life Light Electronic Technology Co., Ltd. | accessdata.fda.gov |
| August 26, 2008 | K081516 | MEDSOURCE CPR MASK WITH & WITHOUT OXYGEN PORT | CBP | Substantially Equivalent | Medsource International, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Cannula, Nasal, Oxygen
- All makers of Generator, Oxygen, Portable
- All makers of Regulator, Pressure, Gas Cylinder
- All makers of Mask, Oxygen
- All makers of Cylinder, Compressed Gas, And Valve
- All makers of Valve, Non-Rebreathing
Updated April 23, 2026. 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.