Osteograf/Ar and Osteograf/Ar+

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K862324 ↗

FDA Product Code

LYC

Device Class

Class II

Regulation

21 CFR Part 872.3930

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Osteograf/Ar+ Alveolar Rid Hydrox 18-40 Mesh

  Class II

  FDA 510(k) K861083 Active Cleared 30 Apr 1986

• Osteograf Ar Alveolar Ridge Hydroxylapatite 18-40

  Class II

  FDA 510(k) K852742 Active Cleared 26 Sep 1985

• Osteograf/Ar Alveolar Rid Hydrox, 18-40 Mesh

  Class II

  FDA 510(k) K861084 Active Cleared 30 Apr 1986

• Osteograf/Ar+ Permaridge Hydroxylapatite, 18-40

  Class II

  FDA 510(k) K862061 Active Cleared 29 Jul 1986

• Additional Clinical Usages for Osteograf/Ar & Ar+

  Class II

  FDA 510(k) K863176 Active Cleared 26 Nov 1986

• Dental Porcelain Powder

  Class II

  FDA 510(k) K810822 Active Cleared 21 Apr 1981