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Sign in to claim this brandHarmar Summit, LLC
US
Last updated May 24, 2026
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. Harmar Summit, LLC is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Harmar Summit, LLC manufacture?
Harmar Summit, LLC specializes in mobility aids for indoor use, including stairlifts designed for fixed staircases, wheelchair/occupant lifts, and assistive passenger lifts. Their product line covers chair-style stairlifts (like the Highlander, Warrior, and Stratos) as well as lifts for transporting occupants between floors (such as the Hercules II). These devices are intended for residential and light-commercial applications.
Where is Harmar Summit, LLC based?
Harmar Summit, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and customer support, as it operates within the FDA’s jurisdiction for device authorization.
Which regulatory registries list Harmar Summit, LLC’s devices?
Harmar Summit, LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, insurers, and regulators, allowing them to verify specific models like the Highlander or Stratos under their assigned UDI codes.
How are Harmar Summit, LLC’s devices classified under FDA regulations?
Harmar Summit, LLC’s devices fall under Class II classification by the FDA. This classification applies to products that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as stairlifts and lifts for occupant transport. Class II devices typically require premarket notification (510(k)) clearance before commercial distribution.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- harmar.com
- —
- —
- [email protected]
- Phone
- +1(800)833-0478
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 144008062
Catalogue (563)
Page 12 of 12| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Highlander | Highlander II | FDA UDI | Class II | Active |
| Hercules Ii | CPL | FDA UDI | Class II | Active |
| Helix | Helix 4 | FDA UDI | Class II | Active |
| Hercules Ii | CPL | FDA UDI | Class II | Active |
| Pinnacle Lite | SL300 | FDA UDI | Class II | Active |
| Hercules Ii | RPL | FDA UDI | Class II | Active |
| Helix | Heim LH | FDA UDI | Class II | Active |
| Highlander | CPL | FDA UDI | Class II | Active |
| Stratos | VPL | FDA UDI | Class II | Active |
| Rave | SL600 | FDA UDI | Class II | Active |
| Highlander | Highlander II | FDA UDI | Class II | Active |
| Highlander | CPL | FDA UDI | Class II | Active |
| Rpl/Cpl Vertical Platform Lifts | K091881 | FDA 510(k) | Class II | Active |
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