Defibtech, LLC: PMA supplement approved for Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, L
Defibtech, LLC (Guilford, Connecticut): PMA supplement approved for Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, L. Dated 103 days ago, it serves as a historical benchmark. Score 30/100. As of 2026-11-04, from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration).
Data as of · Compiled by Zalwin from openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
Free preview: all 8 published fields of this record are shown below. Locked: 3 related CT FdaApprovalPulse records and the 4-column CSV export.
| Field | Value |
|---|---|
| Sponsor | Defibtech, LLC |
| Product | Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, Lifeline/ReviveR VIEW AUTO DDU- |
| Generic / ingredient | Automated external defibrillators (non-wearable) |
| Approval | PMA supplement (device change) |
| Application | P160032 S014 |
| Decided | 2026-07-24 |
| Panel / class | Cardiovascular |
| Sponsor location | Guilford, CT |
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| CRM-ready export with official source URLs | 🔒 Click to unlock → |
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CSV columns: Sponsor · Product · Approval · Decided · official source URL
- Source agency: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration)
- Record date: 2026-07-24
- Data refreshed: 2026-11-04
- Refunds on request within 14 days
Top FdaApprovalPulse records (CT first): Defibtech, LLC · Defibtech, LLC · Defibtech, LLC · Instylla, Inc. · Ventana Medical Systems, Inc. (Roche Tissue Diagnostics) · Browse all by state and category →
LIVE PUBLIC DATA Source: openFDA device PMA and Drugs@FDA endpoints (U.S. Food and Drug Administration) · Last refreshed: Wed, 04 Nov 2026 06:06:18 GMT
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Peer benchmark and outreach value: Defibtech, LLC and 4 Connecticut peers
- Connecticut FdaApprovalPulse records like this one: 4
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every Connecticut peer: $800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
30 / 100 Score
What is the FdaApprovalPulse record for Defibtech, LLC in Guilford, Connecticut?
The FDA approved Lifeline/ReviveR DDU-100, Lifeline/ReviveR AUTO DDU-120, Lifeline/ReviveR VIEW DDU-2300, Lifeline/ReviveR VIEW AUTO DDU- (P160032 S014) for Defibtech, LLC on 2026-07-24: PMA supplement (device change).
How does Defibtech, LLC compare to other Connecticut FdaApprovalPulse records?
It is 103 days old; check the official source for later updates before acting. Its Score of 30/100 is modest; treat it as background rather than a priority.
Defibtech, LLC vs. top 3 peers
| Organization | Location | Record date |
|---|---|---|
| Defibtech, LLC | Guilford, CT | 2026-07-24 |
| Instylla, Inc. | Bedford, MA | 2026-10-23 |
| Ventana Medical Systems, Inc. (Roche Tissue Diagnostics) | Tucson, AZ | 2026-10-23 |
| Cerenovus, Inc. | Miami, FL | 2026-10-23 |
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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.