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EKL — Point, Silver, Endodontic Class I

FDA Device Classification

FDA product code EKL covers "Point, Silver, Endodontic", a Class I medical device regulated under 21 CFR 872.3840. Submissions are reviewed by the Dental panel. At least 3 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
EKL
Device Class
Class I
Regulation Number
872.3840
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K992582pacific implantPACIFIC IMPLANT TITANIUM ENDODONTIC POINTOctober 21, 1999
K961089pulpdentPULPDENT ENDOPREP IIApril 23, 1996
K822568kelleherEAR PROBESSeptember 14, 1982

FDA data resources