Product Code: EMO FDA class 1 21 CFR 872.4565

Knife, Periodontic

Dental

The periodontic knife is a specialized dental instrument used for incision and reshaping of gingival tissue during periodontal surgical procedures such as gingivectomy. It is classified as FDA Class 1, the lowest risk classification, requiring only general controls. The product code is EMO, regulated under 21 CFR 872.4565 in the Dental specialty. No special flags apply to this device.

510(k)s
0
FEI Numbers
56
Registration Numbers
56
Unique Applicants
0
Years Active

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Basic Information

Product Code
EMO
Device Class
FDA class 1
Regulation Number
872.4565
Medical Specialty
Dental
Review Panel
DE
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

FEI Numbers

This FDA classification entry is associated with 56 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 56 registration numbers. Click on an entry to view related FDA registrations.