ELE — Implant, Subperiosteal Class II

FDA Device Classification

FDA product code ELE covers "Implant, Subperiosteal", a Class II medical device regulated under 21 CFR 872.3645. Submissions are reviewed by the Dental panel. Devices under this code are implants. At least 4 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
ELE
Device Class
Class II
Regulation Number
872.3645
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
Yes

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K210228kls-martin l.pKLS Martin IPS PreprostheticJuly 8, 2022
K862926jeneric indSURGICAL VITEXAugust 29, 1986
K843557katechoK-APATITE 20-40 MESH K-APATITE 40-60November 30, 1984
K801208colmedHOLLOW BASKET TITANIUM DENTAL IMPLANTMay 28, 1980