Bioglass Dental Endosseous Ridge Maintainer

K880371 is the FDA 510(k) clearance record for BIOGLASS DENTAL ENDOSSEOUS RIDGE MAINTAINER, a class II device, cleared for American Biomaterials Corp. on 1988-11-18 under FDA product code LYC (Bone Grafting Material, Synthetic). FDA's definition for product code LYC reads: "A synthetic bone grafting material is synthetically-derived device, such as hydroxylapatite, intended to fill, augment, or reconstruct periodontal and or bony defects of the upper or lower jaw". FDA records list 6 510(k) clearances for American Biomaterials Corp., from 1985-01-09 to 1994-07-07. As of 2026-09-10, FDA records show no recalls naming K880371.