Data / Medical devices / United States / Life Spark Medical
Life Spark Medical: FDA-registered device maker in Hurricane, UT, United States, 1 510(k) clearance
Life Spark Medical is registered with the FDA (registration 3040167376) in Hurricane, UT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 24, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3040167376
- Address
- 2430 W 350 N, Hurricane, UT, United States, 84737
- Owner or operator
- Life Spark Medical (10094534)
- Roles
- Manufacturer, Specification developer
- First device listed
- December 5, 2025
- Registered through
- 2026
- Brand names listed
- Smart Check O2
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Gas, Oxygen, Gaseous-Phase | CCL | 2 | Manufacturer, Specification developer | 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 24, 2025 | K250002 | Smart Check O2 (MA0236) | CCL | Substantially Equivalent | Life Spark Medical, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 24, 2025. 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.