Regenafil, Regenaform, Alriva Dbm Paste, Sltiva Dm with Cortical Cancellous Ships, Bioset, Sioset Ic, Rti Allograft Past

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K080418 ↗

FDA Product Code

NUN

Device Class

Class II

Regulation

21 CFR Part 872.3930

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Sterling Interference Screw St

  Class II

  FDA 510(k) K050767 Active Cleared 9 Jun 2005

• Opteform, Osteofil, Rti Allograft Paste Ic, Rti Allograft Strip Ic

  Class II

  FDA 510(k) K043421 Active Cleared 16 Feb 2005

• Sterling If Screw Eyelet, Model CID3936 and Sterling Cross-Pin Eyelet, Model CID3937

  Class II

  FDA 510(k) K063584 Active Cleared 9 May 2007

• Osteofil, Optefil, Regenafil, Rti Allograft Paste

  Class II

  FDA 510(k) K043420 Active Cleared 10 Feb 2005

• Bioset Xc

  Class II

  FDA 510(k) K060180 Active Cleared 6 Sep 2006

• Sterling Interferenc Screw Ht

  Class II

  FDA 510(k) K052405 Active Cleared 16 Nov 2005

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