FDA Device Intelligence
Home › Harmar Summit, LLC › Highlander

Highlander

Harmar Summit, LLC · Model VPLX0600SACI · UDI-DI 00817650026331

PCE
1
510(k) clearances
12
Adverse events (1 deaths)
0
Recalls
12
Facilities

Description

Platform lift,6ft, standard, residential, no hoistway, AC indoor

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.