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

CERAMAFLEX BRACKET SYSTEM

K Number: K950992 · Decision May 3, 1995
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
59
Applicant Total
5
Review Days
61

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
CERAMAFLEX BRACKET SYSTEM
K Number
K950992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.5470
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Tp Orthodontics, Inc.
Date Received
March 3, 1995
Decision Date
May 3, 1995
Product Code
NJM
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
NJM Bracket, Ceramic, Orthodontic

Similar 510(k) Clearances

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

View all

Other Clearances by Tp Orthodontics, Inc.

K Number Device Name
K214054 TP Orthodontics Light-Cure Adhesive System, TP Orthodontics Pre-Applied Adhesive, TP Orthodontics Etchant208520
K193385 TP Orthodontics Clear Aligner System
K111234 CLICK-IT
K952643 RIGHT-ON ADHESIVE BOUDING SYSTEM