Lewis acids are defined as electron pair acceptors. Therefore the examples among the organic compounds would be trimethylboron, tetracyanoethylene, some metal complexes like acetylacetonates (or beta-diketonates in general - does someone remember "shift-reagents" from the dawn of NMR era ?), diethylaluminum chloride, etc.
Alkyl and halo boron and aluminum compounds are great Lewis acids. Though they not strictly "organic" since boron and aluminum are kind of metals, triphenyl carbenium won't act as a great "Lewis acid" so much as it will a hydride abstractor.
Tropylium cation, 7,7,8,8-tetracyanoquinodimethane and tetracyanoethylene ( as Vladimir pointed ) are 100% organic (carbon-centered ) Lewis acids.
Triphenylcarbenium (noted by Brennan) and tricyclopropyl carbenium cations are also stable C-centered Lewis acids, they reacts with pyridine, N-methylimidazole and same bases like other typical metal-centerd Lewis acids - by accepting its lone pair.