Harmar Summit, LLC
Country not established
Harmar Summit, LLC is a medical device manufacturer, with 563 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 563
Registry facts
- Registries
- FDA GUDID 562
- FDA 510(k) 1
- Device classes
- FDA Class II 562
- Identifiers
- DUNS 144008062
What Harmar Summit, LLC makes
Harmar Summit, LLC manufactures stairlifts designed for indoor use, including chair-style stairlifts for fixed staircases, as well as wheelchair and assistive passenger lifts for transporting occupants between floors. Their product line includes models like the Highlander, Warrior, Stratos, and Hercules II, which are intended for residential and light-commercial applications.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database.
Catalogue
Search and filter all 563 devicesShowing 1-50 of 563
Company details
- DUNS number
- 144008062
- Phone
- +1(800)833-0478
Frequently asked questions
How many devices does Harmar Summit, LLC have in the registry?
The registry currently lists 563 devices for Harmar Summit, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harmar Summit, LLC's devices?
Among its 50 most recently registered devices, Harmar Summit, LLC has devices listed in FDA GUDID (50 devices).
What risk classes do Harmar Summit, LLC's devices fall under?
Among its 50 most recently registered devices, the classes recorded for Harmar Summit, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harmar Summit, LLC in the registry?
The most recently registered devices listed for Harmar Summit, LLC include Highlander II, WARRIOR WL600, Stratos VPL and HERCULES II CPL.