- Trust center · Review methodology
How we verify every AED review: sources, not stories.
- Updated · July 2026
- Editorially reviewed
- Standards
- Who we are
- Direct answer
- Editorial methodology · four sources
How we verify every claim: 4 primary sources, every claim dated at capture.
01 · REGULATORY
FDA premarket approval records
02 · MANUFACTURER
Instructions for use + datasheets
04 · MARKET
Dated distributor pricing
- What we do NOT claim
We do not run a hands-on laboratory testing program. We do not have clinicians approving verdicts. We do not publish consumer-review averages, and our editorial scores are labeled as exactly what they are.
Our value is rigorous, dated synthesis of the four public sources above, done consistently across every model, with every check dated. If you need device servicing, contact the manufacturer; if you need medical guidance, consult a licensed clinician.
- The scoring system
What decides a verdict, and by how much?
| Criterion | Weight | What it measures | Public data behind it |
|---|---|---|---|
| Rescuer simplicity | 25% | Can an untrained bystander complete a rescue: prompts, pad design, steps to shock | Manufacturer IFUs, AHA public-access guidance[3] |
| 5-year total cost | 25% | Device + pads + battery + cabinet over 5 years, not sticker price | Dated distributor pricing, manufacturer consumable cycles, our Cost Calculator math |
| Consumable architecture | 20% | How maintenance survives real organizations: expiry-date count, combined cartridges, part availability | Manufacturer cycles, the by-model matrix |
| Durability + environment | 15% | IP rating, temperature range, crush and drop specs for the deployment it serves | Manufacturer datasheets, IEC 60529 definitions[7] |
| Readiness signaling | 15% | Self-test cadence and how clearly a failing unit announces itself | Manufacturer IFUs |
- Scope + cadence
Which models, and how often is it re-checked?
The review set is nine FDA-approved models across the six brands sold through authorized US channels. Named, so the count is checkable:
All verifiable in FDA PMA records
How freshness actually works
- When we are wrong
Corrections and updates: the boring promise that matters
- Every quantitative claim is a cited fact, a labeled estimate, or a calculation with visible inputs; anything that cannot meet one of those three standards does not ship.
- Revenue comes from clearly marked referral links to authorized distributors; no manufacturer pays for placement or sees a verdict early, and rankings never consider referral economics. Clinical framing follows AHA statistics[4].
- Where the right answer is "see your state's statute" or "ask a clinician," the page says so instead of pretending: the law tracker and primary sources exist for exactly that.
How this site is funded
Read before relying on us
- The methodology, applied · Free tools
See the criteria working in the tools.
01 · READ
The Complete Buyer's Guide
02 · MATCH
Find Your Perfect AED
03 · BUDGET
AED Cost Calculator
04 · COUNT
AED Quantity Calculator
- Methodology questions
Asked often, answered plainly
Do you physically test AEDs in a lab?
No, and we say so in the open. The reviews are rigorous syntheses of the four public sources above. Sites that claim testing panels and month-long lab programs rarely show a single photograph of either; we would rather be checkable than impressive.
Are your reviews medically approved?
No clinician signs off on verdicts and we claim no medical approval. Clinical statements cite AHA, CDC, OSHA, and peer-reviewed sources inline so you can verify them where they were published. Our process rules live on the editorial standards page.
How do you make money, and does it touch rankings?
Clearly marked referral links to authorized distributors, and no. No manufacturer pays for placement or previews a verdict, rankings never weigh referral economics, and the same criteria table above governs every pick including the 2026 awards.
Why only nine models?
Because the review set is defined by verifiability: FDA-approved models sold through authorized US channels with current manufacturer documentation. Gray-market imports fail that test and stay out, whatever their price. The set is listed above so the count is checkable, and it grows when a model clears the same bar.
How current is any given page?
Each page carries its update date top and bottom, and every price is shown with the date it was checked. If you catch something stale, the corrections channel gets it corrected in place with the date advanced.
- RegulatoryUS FDA. Automated External Defibrillators overview and premarket approval requirement (effective 2016). fda.gov AEDs
- RegulatoryUS FDA. Premarket Approval (PMA) database. accessdata.fda.gov PMA
- ProgramAmerican Heart Association. Implementing an AED Program, 2023 guide. cpr.heart.org AED guide (PDF)
- ClinicalAmerican Heart Association. Heart Disease and Stroke Statistics, annual update. Circulation. heart.org statistics
- LegalCDC. Public Access Defibrillation State Law Fact Sheet. cdc.gov PAD fact sheet
- RegulatoryUS OSHA. Saving Sudden Cardiac Arrest Victims in the Workplace, Publication 3185. osha.gov 3185 (PDF)
- Standard IEC. IEC 60529: Degrees of protection provided by enclosures (IP Code). webstore.iec.ch