FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

OsteoCentric Dental Implant System

K Number: K230242 · Decision Oct 5, 2023
Classifications
1
FEI Numbers
324
Registration Numbers
324
Same Product Code
1545
Applicant Total
11
Review Days
248

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
OsteoCentric Dental Implant System
K Number
K230242
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3640
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OsteoCentric Technologies
Date Received
January 30, 2023
Decision Date
October 5, 2023
Product Code
DZE
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZE Implant, Endosseous, Root-Form

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DZE), ordered by most recent decision date.

View all

Other Clearances by OsteoCentric Technologies

K Number Device Name
K251913 OsteoCentric® UnifiMI® TCS Plating System
K250494 The OsteoCentric Bone Plate and Screw System
K242691 OsteoCentric Technologies Cannulated Fasteners and Nuts
K230226 Integrity-SI® Fusion System
K230595 OsteoCentric ACL Fixation System
K230764 OsteoCentric Integrated Hip Fastener System
K222512 Integrity-SI Fusion System
K221332 OsteoCentric Spine MIS Pedicle Fastener System
K211290 Cannulated Fasteners and Nuts
K210754 Cannulated Fasteners and Nuts
Search all 11 clearances from OsteoCentric Technologies →