Product Code: EKC FDA class 1 21 CFR 872.4565

Excavator, Dental, Operative

Dental

The Dental Operative Excavator is a hand instrument with a spoon-shaped or hoe-shaped working end used to remove carious dentin, temporary restorations, and debris from prepared tooth cavities in advance of placing a permanent restoration. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EKC, regulated under 21 CFR 872.4565 in the Dental (DE) specialty.

510(k)s
2
FEI Numbers
116
Registration Numbers
116
Unique Applicants
2
Years Active
1

Research product code EKC in seconds

The Research Assistant summarizes clearances, adverse event trends and regulation context for a product code — and cites every record.

Free to try · every answer cites its records

Basic Information

Product Code
EKC
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

510(k) Clearance History

Loading...

Related 510(k) Clearances

This FDA classification is associated with 2 510(k) clearances via K numbers.

K Number Device Name
K851722 1285/5 TO 1295 VARIOUS TYPES OF DENTAL EXCAVATORS
K834055 VANADIUM EXCAVATORS SIZES 0-6

FEI Numbers

This FDA classification entry is associated with 116 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 116 registration numbers. Click on an entry to view related FDA registrations.