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

LUXATEMP ULTRA /STAR

K Number: K101710 · Decision Sep 28, 2010
Classifications
1
FEI Numbers
180
Registration Numbers
180
Same Product Code
188
Applicant Total
28
Review Days
103

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Basic Information

Device Name
LUXATEMP ULTRA /STAR
K Number
K101710
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3770
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dmg USA, Inc.
Date Received
June 17, 2010
Decision Date
September 28, 2010
Product Code
EBG
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
EBG Crown And Bridge, Temporary, Resin

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Other Clearances by Dmg USA, Inc.

K Number Device Name
K171772 Ecosite Bulk Fill
K160443 TempoCem Clear
K130580 RETRACTION PASTE
K110759 TEMPOCEM
K102603 SA FLOWABLE ADHESIVE
K100062 INFILTRATION KIT
K093338 SELF ADHESIVE COMPOSITE LUTING CEMENT
K093587 DENTAL MERCURY
K081493 INFILTRATION KIT
K080480 NANOCOMPOSITE RESTORATIVE KIT
Search all 28 clearances from Dmg USA, Inc. →