Bone Level Tapered Multi-Center Study

Exclusion Criteria

• •Subjects with a systemic disease that would preclude dental implant surgery
• •Subjects with any contraindications for oral surgical procedures
• •Subjects with mucosal diseases (e.g., erosive lichen planus) in the localized area around the study implant site
• •Subjects with a history of local irradiation therapy in the head/neck area
• •Subjects with any untreated endodontic lesions or untreated periodontal disease adjacent to the implant site
• •Subjects receiving, or having a history of receiving, intravenous or subcutaneous antiresorptive agents, such as bisphosphonates
• •Subjects with severe bruxing, parafunctional habits, or temporomandibular joint dysfunction
• •Any implant sites where there will be a buccal dehiscence greater than 3 mm or there will be a fenestration of the implant
• •Subjects with inadequate oral hygiene or who are unmotivated for adequate home care
• •Subjects who have physical or mental handicaps that would interfere with the ability to perform adequate oral hygiene
• •Subjects who are pregnant or intending to become pregnant during the duration of the study
• •Subjects who are heavy smokers (defined as \>10 cigarettes per day or \>1 cigar per day) or chew tobacco
• •Subjects who abuse alcohol or drugs
• •Subjects who have undergone administration of any investigational device within 30 days of enrollment in the study
• •Subjects with conditions or circumstances, in the opinion of the investigator, which would prevent completion of study participation or interfere with analysis of study results, such as history of non-compliance or unreliability