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EKQ – Preparer, Root Canal Endodontic
Preparer, Root Canal Endodontic
FDA product code
EKQ
· Class I (low risk) · 21 CFR 872.4565 ·
Dental
2
510(k) clearances
0
PMA approvals
0
recalls
Manufacturers
Almore Intl., Inc.
1
Syntex Dental Products, Inc.
1
510(k) clearances
510(k)
Device
Applicant
Decision
K832378
Vibratory Endodontic System
EKQ · Traditional
Syntex Dental Products, Inc.
10/04/1983
SE
K801463
OJ-1 Endodonic Root Canal File Holder
EKQ · Traditional
Almore Intl., Inc.
07/21/1980
SE