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

UltraTemp Rez II

K Number: K211237 · Decision Jul 13, 2021
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
103
Review Days
78

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Basic Information

Device Name
UltraTemp Rez II
K Number
K211237
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ultradent Products, Inc.
Date Received
April 26, 2021
Decision Date
July 13, 2021
Product Code
EMA
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
EMA Cement, Dental

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K211905 UltraCal XS
K210550 VALO Grand Corded and Accessory Lenses
K190627 VALO Grand Corded
K173163 ChlorCid, ChlorCid V, ChlorCid Surf
K160551 VALO Grand
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