FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DENTAURUM CERAMIC DEBONDING UNIT

K Number: K902018 · Decision Apr 3, 1991
Classifications
1
FEI Numbers
160
Registration Numbers
160
Same Product Code
30
Applicant Total
24
Review Days
335

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Basic Information

Device Name
DENTAURUM CERAMIC DEBONDING UNIT
K Number
K902018
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Dentauraum, Inc.
Date Received
May 3, 1990
Decision Date
April 3, 1991
Product Code
EKS
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
EKS File, Pulp Canal, Endodontic

Similar 510(k) Clearances

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

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Other Clearances by Dentauraum, Inc.

K Number Device Name
K952870 REMANIUM: CS & G-SOFT
K952867 REMANIUM:GM 700, GM 380, GM 800, GFH
K952866 REMATITAN TITANIUM
K952865 REMANIUM: 200,CS, 380, AND CD
K952868 DENTAURUM JACKET CROWN & ROOT POSTS
K942667 DENT-O-CRYL ORTHODONTIC ACRYLIC
K942666 ORTHALGENAT IMPRESSION MATERIAL
K936151 EXTRAORAL HEADGEAR
K942665 ORTHOCENT: LIQUID AND POWDER
K942668 O-TRAY IMPRESSION TRAYS
Search all 24 clearances from Dentauraum, Inc. →