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Simple Summary: A salivary mucocele is the most common disorder affecting the salivary glands. Saliva leakage from the salivary gland parenchyma and/or from associated duct damage causes a chronic inflammatory process which can occasionally result in osseous metaplasia. Dogs having an ossified sialocele present with a hard, non-fluctuating mass containing a viscous, sticky liquid at centesis. Either radiography or computed tomography can confirm the thick bone-like wall pseudocyst. Surgical excision of both the pseudocyst and the affected salivary gland represents the therapeutic gold standard in these cases. The aim of this study was to report the clinical and diagnostic findings, surgical management and histopathologic report of three cases of cervical sialocele complicated by pseudocapsule osseous metaplasia. Saliva is an irritant of the subcutaneous tissue, thus causing the development of a non-epithelial reactive pseudocapsule. Metaplastic ossification of the pseudocapsule is a condition rarely described in the veterinary literature. The main causes of calcification are trauma, tumours, various chronic inflammatory conditions and fibrodysplasia ossificans progressiva. The aim of the present case series was to describe three dogs affected by a calcified salivary mucocele. The medical records of dogs affected by a cervical sialocele were retrospectively evaluated, and three cases met the inclusion criteria. All the dogs in this study were referred to the Veterinary Teaching Hospital (VTH) of the Department of Veterinary Sciences of the University of Turin (Turin, Italy) for a large solid mass in the intermandibular region. The diagnosis of a mucocele was confirmed clinically by centesis and by radiography or CT. Complete excision of both the pseudocyst and the ipsilateral mandibular/monostomatic sublingual salivary gland was performed in all cases. The histological report showed large areas of bone metaplasia within the pseudocapsule and chronic sialadenitis. Based on this limited case series, complete excision of the pseudocyst and a concurrent sialoadenectomy provided an effective treatment for this rare salivary mucocele disorder. [ABSTRACT FROM AUTHOR]