Data / Medical devices / United States / Essex Industries, Inc
Essex Industries, Inc: FDA-registered device maker in Affton, MO, United States, 3 510(k) clearances
Essex Industries, Inc is registered with the FDA (registration 1937980) in Affton, MO, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated June 29, 2012. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1937980
- Address
- 8007 Chivvis DR., Affton, MO, United States, 63123
- Owner or operator
- Essex Industries, Inc (1937613)
- Roles
- Manufacturer, Remanufacturer
- First device listed
- December 18, 2007
- Registered through
- 2027
- Brand names listed
- BACKPACK MEDICAL OXYGEN SYSTEM (BMOS), MMOS, NEXT GENERATION PORTABLE THERAPEUTIC LIQUID OXYGEN (NPTLOX)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Liquid-Oxygen, Portable | BYJ | 2 | Manufacturer, Remanufacturer | 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 |
|---|---|---|---|---|---|---|
| June 29, 2012 | K113767 | MOUNTED MEDICAL OXYGEN SYSTEM | BYJ | Substantially Equivalent | Essex Industries, Inc. | accessdata.fda.gov |
| July 11, 2007 | K071581 | BACKPACK MEDICAL OXYGEN SYSTEM | BYJ | Substantially Equivalent | Essex Cryogenics of Missouri, Inc. | accessdata.fda.gov |
| March 22, 2004 | K033000 | NEXT GENERATION PORTABLE THERAPEUTIC LIQUID OXYGEN SYSTEM | BYJ | Substantially Equivalent | Essex Cryogenics of Missouri, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 29, 2012. 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.