Data / Medical devices / United States / LifeVac, LLC
LifeVac, LLC: FDA-registered device maker in Nesconset, NY, United States, 1 510(k) clearance
LifeVac, LLC is registered with the FDA (registration 3011053282) in Nesconset, NY, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 4, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011053282
- Address
- 110 Lake Ave South Suite 35, Nesconset, NY, United States, 11767
- Owner or operator
- LifeVac, LLC (10047348)
- Roles
- Manufacturer
- First device listed
- March 5, 2026
- Registered through
- 2026
- Brand names listed
- LifeVac
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Suction Anti-Choking Device As A Second-Line Treatment | QXN | 2 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| March 4, 2026 | DEN250012 | LifeVac | QXN | Unknown | Lifevac, LLC | accessdata.fda.gov |
Updated March 4, 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.