Cyber-Fil Alkenoate Cement Multi-Purpose Kit (23900/23905/23910/23915/23920)

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

510(k) Number

K962733 ↗

FDA Product Code

EMA

Device Class

Class II

Regulation

21 CFR Part 872.3275

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• Inject-R Fill

  Class I

  FDA 510(k) K931742 Active Cleared 27 May 1993

• Nickel-Titanium K-Type File

  Class I

  FDA 510(k) K935542 Active Cleared 3 Jan 1994

• Union Broach Bleaching Light

  Class I

  FDA 510(k) K895174 Active Cleared 13 Apr 1990

• Thermal Pulp Tester

  Class II

  FDA 510(k) K940260 Active Cleared 7 Mar 1994

• Moyco-Edta

  Unclassified

  FDA 510(k) K950365 Active Cleared 27 Apr 1995

• Root Canal Files, Type K

  Class I

  FDA 510(k) K822621 Active Cleared 28 Sep 1982

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