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

DENTAURUM EXPANSION SCREWS

K Number: K935154 · Decision Feb 3, 1994
Classifications
1
FEI Numbers
120
Registration Numbers
120
Same Product Code
4
Applicant Total
24
Review Days
98

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Basic Information

Device Name
DENTAURUM EXPANSION SCREWS
K Number
K935154
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.5410
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Dentauraum, Inc.
Date Received
October 28, 1993
Decision Date
February 3, 1994
Product Code
DYJ
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
DYJ Retainer, Screw Expansion, Orthodontic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DYJ), 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. →