Consistent automatic suction — not user-force dependent.
When a child is choking, your body floods with adrenaline. Fine motor skills degrade. Strength becomes unreliable. Panic is not a side effect — it's the condition. Most anti-choking devices rely on you performing perfectly under pressure.
One motion triggers a built-in automatic mechanism. It doesn't matter how calm you are, how strong you are, or how fast you react. The result is the same every time.
The device should carry the load — not you.
The difference that matters
Plunger-style devices generate suction based on how hard you pull. Under panic, that varies wildly — up to 10× between a calm practitioner and a panicked parent.
lifewand's built-in automatic mechanism generates a consistent, medically-calibrated vacuum every time. There's no technique to master. No force to summon.
External and non-invasive — surface application over mouth and nose. No insertion, no attachments, no assembly required during an emergency.
Built like medical equipment, not a toy.
lifewand vs plunger-style devices
See it work — inside the device
Three steps. That's it.
Place the device on the cocking strip on a flat, stable surface.
Lean over it and press down with your body weight to compress the spring mechanism.
Press the trigger. The device automatically generates a precise ~3.2 bar vacuum to clear the obstruction.
Quick instructions
Complete instructions — watch once after purchase
One purpose per device
Each lifewand is purpose-built for its age group. Not a universal device with attachments — a dedicated instrument.
Ages 12 and over
Full mask geometry optimised for adult facial anatomy. Maximum vacuum calibration for adult airway dimensions.
Ages 1–11
Smaller mask and calibrated vacuum level for children's airways. Designed so the seal works without excessive force.
Under 12 months
The smallest mask geometry, with a gentle vacuum calibration safe for infant airways and facial structure.
Our Quality Management System is certified to the international standard for medical device manufacturers.
Lifewand Ltd. is a registered FDA medical device establishment (No. 3015168845). Devices are listed with the FDA, valid through 2026.
CE marking (EU/EEA), Health Canada, and AMAR (Israel) submissions are active and in progress.
The device has been tested against the international standard for airway clearance device performance.
If you use your lifewand in a real emergency, contact us and we will send you a replacement at no charge. No questions. No charge.
Availability
lifewand is currently available in Canada via Amazon. Regulatory submissions for Israel and the EU are active and in progress.
Regulatory submissions are active. Sign up below to be notified when lifewand launches in your country.
Get notifiedInterested in distributing lifewand in your country? See distributor information →
Partner with us
We are actively seeking distribution partners in Israel, EU, and beyond — one committed partner per territory.
We work with one committed partner per market. Protect your investment with territorial exclusivity and a long-term partnership built on mutual growth.
CE marking (EU/EEA), AMAR (Israel), and Health Canada submissions are active. We provide all technical files, labeling, and regulatory documentation.
ISO 13485 certified. Tested to ISO 18190. A credible, documented product ready for institutional and retail channels.
Sign up for updates on availability, new markets, and distributor opportunities.
Distributor enquiries, press, or support — we read every message.
You can also reach us directly at marketing@lifewand.com
About us
Extralife Ltd. was founded in Israel with one mission: to build a reliable, engineered device that clears airway obstructions — and works the same every time, regardless of who is holding it or how panicked they are.
We are a medical device manufacturer. Our Quality Management System is certified to ISO 13485 by the Standards Institution of Israel (SII). Our device is tested to ISO 18190, the international standard for airway clearance device performance. Regulatory submissions are active in three markets: Israel (AMAR), EU (CE marking), and Canada (Health Canada).
We believe that reliable emergency tools should not depend on geography — and we are building the partnerships to make that possible.