The interfacial behavior of third and fourth generations of hyperbranched polyesters (HBP3 and HBP4) with 32 and 64 hydroxyl-terminal groups was studied with scanning probe microscopy. The molecular adsorption on a bare silicon surface of both hyperbranched polymers was described in the terms of the Langmuir isotherm. A higher adsorption amount under an identical adsorption condition was found for lower generation HPB3. The shape of HBP3 molecules within an adsorbed layer evolved from a pancake with a thickness less than 1 nm for very low surface coverage to densely packed wormlike bilayer structures with a thickness of about 3 nm for the highest surface coverage. The molecules of the fourth generation, HBP4, hold a stable, close-to-spherical shape with a diameter of 2.5 nm throughout the entire range of surface coverage including both dense monolayers and isolated molecules. High intramolecular flexibility of HBP3 molecules as compared with constrained mobility of bulkier branches of HBP4 is considered to be responsible for different surface behavior.