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

TEMPOCEM

K Number: K110759 · Decision Jun 10, 2011
Classifications
1
FEI Numbers
71
Registration Numbers
71
Same Product Code
10
Applicant Total
28
Review Days
84

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Basic Information

Device Name
TEMPOCEM
K Number
K110759
Device Class
FDA class 1
Clearance Type
Abbreviated
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dmg USA, Inc.
Date Received
March 18, 2011
Decision Date
June 10, 2011
Product Code
EMB
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
EMB Zinc Oxide Eugenol

Similar 510(k) Clearances

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Other Clearances by Dmg USA, Inc.

K Number Device Name
K171772 Ecosite Bulk Fill
K160443 TempoCem Clear
K130580 RETRACTION PASTE
K102603 SA FLOWABLE ADHESIVE
K101710 LUXATEMP ULTRA /STAR
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. →