Med-Life, Inc.
United StatesFDA 510(k) applicant, unverified FDA
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
Catalogue
Head-Up Supine Safety Support Cushion Ref K821306
Anesthecache Ref K821307
FDA establishments
- Medlife Ltd. IL
What Med-Life, Inc. makes
Med-Life, Inc. manufactures patient safety and respiratory support devices, including the Head-Up Supine Safety Support Cushion for hospital beds, the Anesthecache—a device for anesthetic gas scavenging, and the Med-Life Emergency Oxygen Regreather/Resuscitator for emergency oxygen delivery and patient resuscitation.
The company’s portfolio includes Class I and Class II medical devices, with products listed under the FDA’s 510(k) clearance pathway. These devices are regulated under US medical device laws and are based in the United States.
Frequently asked questions
How many devices does Med-Life, Inc. have in the registry?
The registry currently lists 3 devices for Med-Life, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-Life, Inc.'s devices?
Among its 3 most recently registered devices, Med-Life, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Med-Life, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Med-Life, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-Life, Inc. in the registry?
The most recently registered devices listed for Med-Life, Inc. include HEAD-UP SUPINE SAFETY SUPPORT CUSHION, ANESTHECACHE and MED-LIFE EMERGENCY OXYGEN REGREATHER/RESUSCITATOR.
Which FDA establishments are linked to Med-Life, Inc.?
1 FDA establishment is linked to Med-Life, Inc. in the registry; they are listed on the company page.