- Trust center · Editorial standards
The rules behind every page we publish.
- Updated · August 2026
- How reviews are verified
- Who we are
- Direct answer
- Editorial methodology · four sources
Under this standard, every number fits one of three buckets, or it does not ship.
01 · CITED FACT
Traced to a primary source
02 · LABELED ESTIMATE
Marked as an estimate, with its basis
03 · SOURCED CALCULATION
Math with visible inputs
BANNED OUTRIGHT
What never ships
- What editorial review is NOT
The Editorially reviewed label identifies a page presented under these written editorial standards. It is an editorial label, not medical review, clinical sign-off, certification, or legal advice.
For clinical questions consult a licensed clinician; for legal obligations, your state’s statute controls, and our law tracker links the primary text.
- Sourcing rules
Which sources qualify, and for what?
| Source class | Examples | Used for |
|---|---|---|
| Regulatory | FDA premarket approval records, FDA recall notices | Approval status, recall status, the reviewed set |
| Manufacturer | Instructions for use, datasheets, official support pages | Specifications, consumable cycles, warranties, pediatric options |
| Clinical + safety | AHA, CDC, OSHA, NEJM, JAMA, Circulation | Survival statistics, placement guidance, workplace rules |
| Legislative | State statute text, federal code | Legal claims, linked to the statute itself |
| Market | Authorized US distributor listings, dated at capture | Prices, availability, package contents |
Regulatory claims are checked against FDA records. The FDA requires current automated external defibrillators and necessary AED accessories to obtain Premarket Approval. We use the applicable PMA record as evidence of current FDA approval. Historical 510(k) records may provide regulatory background, but we do not treat an older 510(k) record as proof that an AED or necessary accessory is currently approved for marketing. Reference: FDA, Automated External Defibrillators (AEDs).
For device specifications and instructions, we prioritize the current manufacturer manual, instructions for use, and specification sheet. For regulatory status, recalls, and legal requirements, the applicable government record takes priority. When reliable sources conflict, we disclose the conflict or remove the claim until it can be resolved. We place citations beside the material claims they support and avoid using a source as evidence for claims it does not establish.
FDA approval applies to the AED model and configuration covered by the approval. It does not verify the condition, maintenance history, remaining consumable life, seller inspection, included supplies, or usability of an individual used device.
- The review pipeline
How content is reviewed under this standard
- Draft against the whitelist. Claims are written from the source classes above, with links captured at writing time.
- Bucket check. Quantitative claims reviewed under this standard are classified into one of the three buckets; anything unclassifiable is cut.
- Banned-claim gate. A written checklist screens for the banned list above plus terminology errors, including FDA approval wording, since AED systems require premarket approval, not 510(k) clearance.
- Dating. Prices and statuses reviewed under this standard get the date they were checked; the page gets a visible update date.
- Ongoing verification. We conduct dated verification passes for recall status and pricing, and findings from those passes feed corrections. Reader reports enter the same path through the corrections route.
Editorial review is not medical review, and this site does not provide medical advice. Our content does not replace manufacturer instructions, formal emergency-response training, or guidance from qualified professionals.
- Money + conflicts
How this site earns, stated plainly
Per FTC endorsement guidance
The firewall rules
- Corrections + updates
When we are wrong, this is what happens
Open to anyone
In place, dated, noted
- Standards questions
Asked often, answered plainly
What does the Editorially reviewed label mean?
The label means the page is presented under these written editorial standards. It is an editorial label, not medical review, clinical sign-off, certification, or legal advice.
Who is "the editorial team"?
The publisher and editors identified on the about page, which states ownership, purpose, and our commercial relationships. We name no experts we do not have.
Why should I trust a site funded by referral fees?
Do not trust; verify. Material factual claims should be traceable to an identified source you can check, the scoring criteria are published, the disclosure above says exactly where money comes from, and the corrections route is public. The structure is designed so you never have to take our word for anything.
How current is any page?
The update date marks the page itself: it advances when the page last changed substantively. Individual prices and statuses carry their own check dates where shown. We conduct dated verification passes for recall status and pricing, and older pages are brought under this standard as they are re-verified. Anything stale you catch first goes through the corrections route.
- RegulatoryUS FTC. Guides Concerning the Use of Endorsements and Testimonials in Advertising (16 CFR Part 255). ftc.gov endorsement guides
- RegulatoryUS FDA. Automated External Defibrillators and Premarket Approval requirement. fda.gov AEDs
- ClinicalAmerican Heart Association. CPR and AED resources. cpr.heart.org