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510(k) K992416

PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE by Usbiomaterials Corp. — Product Code LYC

K992416 is an FDA 510(k) premarket notification submitted by Usbiomaterials Corp. for the device "PERIOGLAS- BIOGLASS BONE GRAFT PARTICULATE". The FDA issued a decision of Substantially Equivalent on October 15, 1999. The device falls under product code LYC (Bone Grafting Material, Synthetic), a Class II device regulated under 21 CFR 872.3930. Usbiomaterials Corp. has at least 4 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 15, 1999
Date Received
July 20, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Bone Grafting Material, Synthetic
Device Class
Class II
Regulation Number
872.3930
Review Panel
DE
Submission Type

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.

Other clearances by Usbiomaterials Corp.

  • K024343 — BUTLER GUM PROPHY PASTE WITH NOVAMIN (July 11, 2003)
  • K000149 — NOVABONE-BIOGLASS BONE GRAFT PARTICULATE (February 7, 2000)
  • K962494 — PERIOGLAS - BIOGLASS BONE GRAFT PARTICULATE (September 20, 1996)
  • K930115 — PERIOGLASS (November 4, 1993)

Other clearances for product code LYC

  • K253317 — Cytrans™ Elashield (July 6, 2026)
  • K253883 — Bonalive Maxillofacial (May 14, 2026)
  • K251818 — BONTREE PLUS (March 6, 2026)
  • K244006 — FG Bone Graft M (September 17, 2025)
  • K243745 — FG Bone Graft B (August 29, 2025)
  • K241186 — Synthetic Bone Graft Particulate (February 21, 2025)
  • K213260 — CMFlexTM (December 30, 2022)
  • K202675 — InRoad® Dental Synthetic Bone Graft (March 4, 2022)
  • K201546 — OsOpia Synthetic Bone Void Filler (October 2, 2020)
  • K201051 — Straumann BoneCeramic (September 24, 2020)

FDA data resources