820/1 to 820/51 Various Types Bone Rongeurs

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K851714 ↗

FDA Product Code

EMM

Device Class

Class I

Regulation

21 CFR Part 872.4565

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

• 7-120, 7-130, 7-140, 7-150, 9-151 to 168, 9-171 to 1

  Class I

  FDA 510(k) K851751 Active Cleared 20 Jun 1985

• 13-270 Kilner Scissors

  Not classified

  FDA 510(k) K851760 Active Cleared 20 Jun 1985

• 600/203 to 650/74XN Various Types of Dent Extracti

  Class I

  FDA 510(k) K851712 Active Cleared 11 Jun 1985

• 19-790 to 19-1042 Dressing/Sponge Forceps

  Class I

  FDA 510(k) K851775 Active Cleared 11 Jun 1985

• 13-320, 13-330 Two Types Nazal Scissors-Heyman, Beck

  Class I

  FDA 510(k) K851763 Active Cleared 11 Jun 1985

• 15-490 to 15-520 Various Splinter Forceps Peet, St

  Class I

  FDA 510(k) K851771 Active Cleared 20 Jun 1985

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