# Defibtech, LLC: PMA supplement approved for Defibtech Lifeline; Defibtech Lifeline AUTO; Defibtech Lifeline VIEW; Defibtech Lifeline V

**Score:** 30/100

| Field | Value |
|---|---|
| Sponsor | Defibtech, LLC |
| Product | Defibtech Lifeline; Defibtech Lifeline AUTO; Defibtech Lifeline VIEW; Defibtech Lifeline VIEW AUTO; Defibtech Lifeline E |
| Generic / ingredient | Automated external defibrillators (non-wearable) |
| Approval | PMA supplement (device change) |
| Application | P160032 S015 |
| Decided | 2026-06-16 |
| Panel / class | Cardiovascular |
| Sponsor location | Guilford, CT |

## Why this score


Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P160032S015). Last refreshed: 2026-11-04T06:06:18.796Z.
From openFDA (PMA and Drugs@FDA). openFDA can lag FDA decisions by days to weeks. Drug supplement types follow the FDA submission class (labeling and REMS, manufacturing/CMC, efficacy, other). Company and product level only. Verify on FDA databases before relying on an approval.