EMOClass I

Knife, Periodontic

21 CFR 872.4565 / Dental

EMO is the FDA product code for Knife, Periodontic, a class I device type, regulated under 21 CFR 872.4565. As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: EMO
Device name: Knife, Periodontic
Regulation: 21 CFR 872.4565
Device class: Class I
Review panel: Dental
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 59 companies shown, in name order

Recent clearances

Product code EMO

FDA records hold no clearances under product code EMO.

Recent recalls

Product code EMO

Z-1464-2018Class IIThe product inside the package is incorrect. A single blade shoe was mistakenly packaged instead of a double blade.Ace Surgical Supply Co., Inc. / initiated 2018-03-28 / 6

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)